Canonical Allele Identifier: CA2091549678
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51958270_51958271delinsCT , CM000675.2:g.51958270_51958271delinsCT GRCh38
NC_000013.10:g.52532406_52532407delinsCT , CM000675.1:g.52532406_52532407delinsCT GRCh37
NC_000013.9:g.51430407_51430408delinsCT NCBI36
NG_008806.1:g.58224_58225delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*188+40_*188+41delinsAG ENSP00000489512.2:n.*188+40_*188+41delins...
ENST00000673864.2:c.*1099+40_*1099+41delinsAG ENSP00000501045.2:n.*1099+40_*1099+41deli...
ENST00000674147.2:c.1870-664_1870-663delinsAG ENSP00000500964.2:n.1870-664_1870-663deli...
ENST00000242839.10:c.2355+40_2355+41delinsAG MANE Select ENSP00000242839.5:n.2355+40_2355+41delins...
ENST00000344297.9:c.1870-664_1870-663delinsAG ENSP00000342559.5:n.1870-664_1870-663deli...
ENST00000400366.6:c.2022+40_2022+41delinsAG ENSP00000383217.3:n.2022+40_2022+41delins...
ENST00000448424.7:c.2103+40_2103+41delinsAG ENSP00000416738.3:n.2103+40_2103+41delins...
ENST00000673772.1:c.2122-664_2122-663delinsAG ENSP00000501168.1:n.2122-664_2122-663deli...
ENST00000674147.1:c.1426-664_1426-663delinsAG ENSP00000500964.1:n.1426-664_1426-663deli...
ENST00000242839.8:c.2355+40_2355+41delinsAG ENSP00000242839.4:n.2355+40_2355+41delins...
ENST00000344297.8:c.1870-664_1870-663delinsAG ENSP00000342559.5:n.1870-664_1870-663deli...
ENST00000400366.5:c.2022+40_2022+41delinsAG ENSP00000383217.3:n.2022+40_2022+41delins...
ENST00000400370.8:c.1286-8110_1286-8109delinsAG ENSP00000383221.3:n.1286-8110_1286-8109de...
ENST00000418097.7:c.2355+40_2355+41delinsAG ENSP00000393343.2:n.2355+40_2355+41delins...
ENST00000448424.6:c.2122-664_2122-663delinsAG ENSP00000416738.2:n.2122-664_2122-663deli...
ENST00000634296.1:c.316+40_316+41delinsAG
ENST00000634308.1:c.2122-664_2122-663delinsAG ENSP00000489234.1:n.2122-664_2122-663deli...
ENST00000634620.1:n.2490_2491delinsAG
ENST00000634810.1:n.1700+40_1700+41delinsAG
ENST00000634844.1:c.2211+40_2211+41delinsAG ENSP00000489398.1:n.2211+40_2211+41delins...
ENST00000635406.1:n.212-11793_212-11792delinsAG
NM_000053.3:c.2355+40_2355+41delinsAG NP_000044.2:n.2355+40_2355+41delinsAG
NM_001005918.2:c.1870-664_1870-663delinsAG NP_001005918.1:n.1870-664_1870-663delinsA...
NM_001243182.1:c.2022+40_2022+41delinsAG NP_001230111.1:n.2022+40_2022+41delinsAG
XM_005266423.2:c.2259+40_2259+41delinsAG XP_005266480.1:n.2259+40_2259+41delinsAG
XM_005266424.3:c.2259+40_2259+41delinsAG XP_005266481.1:n.2259+40_2259+41delinsAG
XM_005266427.2:c.2122-664_2122-663delinsAG XP_005266484.1:n.2122-664_2122-663delinsA...
XM_005266428.1:c.2103+40_2103+41delinsAG XP_005266485.1:n.2103+40_2103+41delinsAG
XM_005266430.3:c.2355+40_2355+41delinsAG XP_005266487.1:n.2355+40_2355+41delinsAG
XM_005266431.2:c.2319+40_2319+41delinsAG XP_005266488.1:n.2319+40_2319+41delinsAG
XM_005266432.2:c.1870-664_1870-663delinsAG XP_005266489.1:n.1870-664_1870-663delinsA...
XM_006719837.2:c.2259+40_2259+41delinsAG XP_006719900.1:n.2259+40_2259+41delinsAG
XM_006719838.1:c.171+40_171+41delinsAG XP_006719901.1:n.171+40_171+41delinsAG
XM_006719839.1:c.171+40_171+41delinsAG XP_006719902.1:n.171+40_171+41delinsAG
XM_011535117.1:c.2259+40_2259+41delinsAG XP_011533419.1:n.2259+40_2259+41delinsAG
XM_011535118.1:c.2355+40_2355+41delinsAG XP_011533420.1:n.2355+40_2355+41delinsAG
XM_011535119.1:c.2355+40_2355+41delinsAG XP_011533421.1:n.2355+40_2355+41delinsAG
XM_011535120.1:c.1941+40_1941+41delinsAG XP_011533422.1:n.1941+40_1941+41delinsAG
XM_011535121.1:c.2355+40_2355+41delinsAG XP_011533423.1:n.2355+40_2355+41delinsAG
XM_011535122.1:c.1023+40_1023+41delinsAG XP_011533424.1:n.1023+40_1023+41delinsAG
XR_941601.1:n.2574+40_2574+41delinsAG
XR_941602.1:n.2574+40_2574+41delinsAG
XR_941603.1:n.2574+40_2574+41delinsAG
XR_941604.1:n.2574+40_2574+41delinsAG
NM_001330578.1:c.2122-664_2122-663delinsAG NP_001317507.1:n.2122-664_2122-663delinsA...
NM_001330579.1:c.2103+40_2103+41delinsAG NP_001317508.1:n.2103+40_2103+41delinsAG
XM_005266424.4:c.2259+40_2259+41delinsAG XP_005266481.1:n.2259+40_2259+41delinsAG
XM_005266430.4:c.2355+40_2355+41delinsAG XP_005266487.1:n.2355+40_2355+41delinsAG
XM_005266431.4:c.2319+40_2319+41delinsAG XP_005266488.1:n.2319+40_2319+41delinsAG
XM_006719837.3:c.2259+40_2259+41delinsAG XP_006719900.1:n.2259+40_2259+41delinsAG
XM_011535117.3:c.2259+40_2259+41delinsAG XP_011533419.1:n.2259+40_2259+41delinsAG
XM_017020627.1:c.2259+40_2259+41delinsAG XP_016876116.1:n.2259+40_2259+41delinsAG
NM_000053.4:c.2355+40_2355+41delinsAG MANE Select NP_000044.2:n.2355+40_2355+41delinsAG
NM_001005918.3:c.1870-664_1870-663delinsAG NP_001005918.1:n.1870-664_1870-663delinsA...
NM_001330579.2:c.2103+40_2103+41delinsAG NP_001317508.1:n.2103+40_2103+41delinsAG
NM_001243182.2:c.2022+40_2022+41delinsAG NP_001230111.1:n.2022+40_2022+41delinsAG
NM_001330578.2:c.2122-664_2122-663delinsAG NP_001317507.1:n.2122-664_2122-663delinsA...