Canonical Allele Identifier: CA2623114957

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51958235-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51958238del , CM000675.2:g.51958238del	GRCh38
NC_000013.10:g.52532374del , CM000675.1:g.52532374del	GRCh37
NC_000013.9:g.51430375del	NCBI36
NG_008806.1:g.58259del

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*188+75del	ENSP00000489512.2:n.*188+75del
ENST00000673864.2:c.*1099+75del	ENSP00000501045.2:n.*1099+75del
ENST00000674147.2:c.1870-629del	ENSP00000500964.2:n.1870-629del
ENST00000242839.10:c.2355+75del MANE Select	ENSP00000242839.5:n.2355+75del
ENST00000344297.9:c.1870-629del	ENSP00000342559.5:n.1870-629del
ENST00000400366.6:c.2022+75del	ENSP00000383217.3:n.2022+75del
ENST00000448424.7:c.2103+75del	ENSP00000416738.3:n.2103+75del
ENST00000673772.1:c.2122-629del	ENSP00000501168.1:n.2122-629del
ENST00000674147.1:c.1426-629del	ENSP00000500964.1:n.1426-629del
ENST00000242839.8:c.2355+75del	ENSP00000242839.4:n.2355+75del
ENST00000344297.8:c.1870-629del	ENSP00000342559.5:n.1870-629del
ENST00000400366.5:c.2022+75del	ENSP00000383217.3:n.2022+75del
ENST00000400370.8:c.1286-8075del	ENSP00000383221.3:n.1286-8075del
ENST00000418097.7:c.2355+75del	ENSP00000393343.2:n.2355+75del
ENST00000448424.6:c.2122-629del	ENSP00000416738.2:n.2122-629del
ENST00000634296.1:c.316+75del
ENST00000634308.1:c.2122-629del	ENSP00000489234.1:n.2122-629del
ENST00000634620.1:n.2525del
ENST00000634810.1:n.1700+75del
ENST00000634844.1:c.2211+75del	ENSP00000489398.1:n.2211+75del
ENST00000635406.1:n.212-11758del
NM_000053.3:c.2355+75del	NP_000044.2:n.2355+75del
NM_001005918.2:c.1870-629del	NP_001005918.1:n.1870-629del
NM_001243182.1:c.2022+75del	NP_001230111.1:n.2022+75del
XM_005266423.2:c.2259+75del	XP_005266480.1:n.2259+75del
XM_005266424.3:c.2259+75del	XP_005266481.1:n.2259+75del
XM_005266427.2:c.2122-629del	XP_005266484.1:n.2122-629del
XM_005266428.1:c.2103+75del	XP_005266485.1:n.2103+75del
XM_005266430.3:c.2355+75del	XP_005266487.1:n.2355+75del
XM_005266431.2:c.2319+75del	XP_005266488.1:n.2319+75del
XM_005266432.2:c.1870-629del	XP_005266489.1:n.1870-629del
XM_006719837.2:c.2259+75del	XP_006719900.1:n.2259+75del
XM_006719838.1:c.171+75del	XP_006719901.1:n.171+75del
XM_006719839.1:c.171+75del	XP_006719902.1:n.171+75del
XM_011535117.1:c.2259+75del	XP_011533419.1:n.2259+75del
XM_011535118.1:c.2355+75del	XP_011533420.1:n.2355+75del
XM_011535119.1:c.2355+75del	XP_011533421.1:n.2355+75del
XM_011535120.1:c.1941+75del	XP_011533422.1:n.1941+75del
XM_011535121.1:c.2355+75del	XP_011533423.1:n.2355+75del
XM_011535122.1:c.1023+75del	XP_011533424.1:n.1023+75del
XR_941601.1:n.2574+75del
XR_941602.1:n.2574+75del
XR_941603.1:n.2574+75del
XR_941604.1:n.2574+75del
NM_001330578.1:c.2122-629del	NP_001317507.1:n.2122-629del
NM_001330579.1:c.2103+75del	NP_001317508.1:n.2103+75del
XM_005266424.4:c.2259+75del	XP_005266481.1:n.2259+75del
XM_005266430.4:c.2355+75del	XP_005266487.1:n.2355+75del
XM_005266431.4:c.2319+75del	XP_005266488.1:n.2319+75del
XM_006719837.3:c.2259+75del	XP_006719900.1:n.2259+75del
XM_011535117.3:c.2259+75del	XP_011533419.1:n.2259+75del
XM_017020627.1:c.2259+75del	XP_016876116.1:n.2259+75del
NM_000053.4:c.2355+75del MANE Select	NP_000044.2:n.2355+75del
NM_001005918.3:c.1870-629del	NP_001005918.1:n.1870-629del
NM_001330579.2:c.2103+75del	NP_001317508.1:n.2103+75del
NM_001243182.2:c.2022+75del	NP_001230111.1:n.2022+75del
NM_001330578.2:c.2122-629del	NP_001317507.1:n.2122-629del