Canonical Allele Identifier: CA2623118592
Gene: ATP7B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950173_51950174insC , CM000675.2:g.51950173_51950174insC GRCh38
NC_000013.10:g.52524309_52524310insC , CM000675.1:g.52524309_52524310insC GRCh37
NC_000013.9:g.51422310_51422311insC NCBI36
NG_008806.1:g.66321_66322insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*409-13_*409-12insG ENSP00000489512.2:n.*409-13_*409-12insG
ENST00000673864.2:c.*1320-13_*1320-12insG ENSP00000501045.2:n.*1320-13_*1320-12insG
ENST00000674147.2:c.2090-13_2090-12insG ENSP00000500964.2:n.2090-13_2090-12insG
ENST00000242839.10:c.2576-13_2576-12insG MANE Select ENSP00000242839.5:n.2576-13_2576-12insG
ENST00000344297.9:c.2090-13_2090-12insG ENSP00000342559.5:n.2090-13_2090-12insG
ENST00000400366.6:c.2243-13_2243-12insG ENSP00000383217.3:n.2243-13_2243-12insG
ENST00000448424.7:c.2324-13_2324-12insG ENSP00000416738.3:n.2324-13_2324-12insG
ENST00000673772.1:c.2342-13_2342-12insG ENSP00000501168.1:n.2342-13_2342-12insG
ENST00000674147.1:c.1646-13_1646-12insG ENSP00000500964.1:n.1646-13_1646-12insG
ENST00000242839.8:c.2576-13_2576-12insG ENSP00000242839.4:n.2576-13_2576-12insG
ENST00000344297.8:c.2090-13_2090-12insG ENSP00000342559.5:n.2090-13_2090-12insG
ENST00000400366.5:c.2243-13_2243-12insG ENSP00000383217.3:n.2243-13_2243-12insG
ENST00000400370.8:c.1286-13_1286-12insG ENSP00000383221.3:n.1286-13_1286-12insG
ENST00000418097.7:c.2576-13_2576-12insG ENSP00000393343.2:n.2576-13_2576-12insG
ENST00000448424.6:c.2342-13_2342-12insG ENSP00000416738.2:n.2342-13_2342-12insG
ENST00000634296.1:c.537-13_537-12insG
ENST00000634308.1:c.2342-13_2342-12insG ENSP00000489234.1:n.2342-13_2342-12insG
ENST00000634620.1:n.3374-13_3374-12insG
ENST00000634810.1:n.1921-13_1921-12insG
ENST00000634844.1:c.2432-13_2432-12insG ENSP00000489398.1:n.2432-13_2432-12insG
ENST00000635406.1:n.212-3696_212-3695insG
NM_000053.3:c.2576-13_2576-12insG NP_000044.2:n.2576-13_2576-12insG
NM_001005918.2:c.2090-13_2090-12insG NP_001005918.1:n.2090-13_2090-12insG
NM_001243182.1:c.2243-13_2243-12insG NP_001230111.1:n.2243-13_2243-12insG
XM_005266423.2:c.2480-13_2480-12insG XP_005266480.1:n.2480-13_2480-12insG
XM_005266424.3:c.2480-13_2480-12insG XP_005266481.1:n.2480-13_2480-12insG
XM_005266427.2:c.2342-13_2342-12insG XP_005266484.1:n.2342-13_2342-12insG
XM_005266428.1:c.2324-13_2324-12insG XP_005266485.1:n.2324-13_2324-12insG
XM_005266430.3:c.2576-13_2576-12insG XP_005266487.1:n.2576-13_2576-12insG
XM_005266431.2:c.2540-13_2540-12insG XP_005266488.1:n.2540-13_2540-12insG
XM_005266432.2:c.2090-13_2090-12insG XP_005266489.1:n.2090-13_2090-12insG
XM_006719837.2:c.2480-13_2480-12insG XP_006719900.1:n.2480-13_2480-12insG
XM_006719838.1:c.392-13_392-12insG XP_006719901.1:n.392-13_392-12insG
XM_006719839.1:c.392-13_392-12insG XP_006719902.1:n.392-13_392-12insG
XM_011535117.1:c.2480-13_2480-12insG XP_011533419.1:n.2480-13_2480-12insG
XM_011535118.1:c.2576-13_2576-12insG XP_011533420.1:n.2576-13_2576-12insG
XM_011535119.1:c.2576-13_2576-12insG XP_011533421.1:n.2576-13_2576-12insG
XM_011535120.1:c.2162-13_2162-12insG XP_011533422.1:n.2162-13_2162-12insG
XM_011535121.1:c.2576-13_2576-12insG XP_011533423.1:n.2576-13_2576-12insG
XM_011535122.1:c.1244-13_1244-12insG XP_011533424.1:n.1244-13_1244-12insG
XR_941601.1:n.2795-13_2795-12insG
XR_941602.1:n.2795-13_2795-12insG
XR_941603.1:n.2795-13_2795-12insG
XR_941604.1:n.2795-13_2795-12insG
NM_001330578.1:c.2342-13_2342-12insG NP_001317507.1:n.2342-13_2342-12insG
NM_001330579.1:c.2324-13_2324-12insG NP_001317508.1:n.2324-13_2324-12insG
XM_005266424.4:c.2480-13_2480-12insG XP_005266481.1:n.2480-13_2480-12insG
XM_005266430.4:c.2576-13_2576-12insG XP_005266487.1:n.2576-13_2576-12insG
XM_005266431.4:c.2540-13_2540-12insG XP_005266488.1:n.2540-13_2540-12insG
XM_006719837.3:c.2480-13_2480-12insG XP_006719900.1:n.2480-13_2480-12insG
XM_011535117.3:c.2480-13_2480-12insG XP_011533419.1:n.2480-13_2480-12insG
XM_017020627.1:c.2480-13_2480-12insG XP_016876116.1:n.2480-13_2480-12insG
NM_000053.4:c.2576-13_2576-12insG MANE Select NP_000044.2:n.2576-13_2576-12insG
NM_001005918.3:c.2090-13_2090-12insG NP_001005918.1:n.2090-13_2090-12insG
NM_001330579.2:c.2324-13_2324-12insG NP_001317508.1:n.2324-13_2324-12insG
NM_001243182.2:c.2243-13_2243-12insG NP_001230111.1:n.2243-13_2243-12insG
NM_001330578.2:c.2342-13_2342-12insG NP_001317507.1:n.2342-13_2342-12insG