Canonical Allele Identifier: CA2091566149
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946338G= , CM000675.2:g.51946338G= GRCh38
NC_000013.10:g.52520474G= , CM000675.1:g.52520474G= GRCh37
NC_000013.9:g.51418475G= NCBI36
NG_008806.1:g.70157C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*839C= ENSP00000489512.2:n.*839C=
ENST00000673864.2:c.*1750C= ENSP00000501045.2:n.*1750C=
ENST00000674147.2:c.2385C= ENSP00000500964.2:p.Ala795=
ENST00000242839.10:c.3006C= MANE Select ENSP00000242839.5:p.Ala1002=
ENST00000344297.9:c.2385C= ENSP00000342559.5:p.Ala795=
ENST00000400366.6:c.2673C= ENSP00000383217.3:p.Ala891=
ENST00000448424.7:c.2754C= ENSP00000416738.3:p.Ala918=
ENST00000673772.1:c.2772C= ENSP00000501168.1:p.Ala924=
ENST00000673867.1:n.1153C=
ENST00000674126.1:n.3369C=
ENST00000674147.1:c.1941C= ENSP00000500964.1:p.Ala647=
ENST00000242839.8:c.3006C= ENSP00000242839.4:p.Ala1002=
ENST00000344297.8:c.2385C= ENSP00000342559.5:p.Ala795=
ENST00000400366.5:c.2673C= ENSP00000383217.3:p.Ala891=
ENST00000400370.8:c.1716C= ENSP00000383221.3:p.Ala572=
ENST00000418097.7:c.2866-2047C= ENSP00000393343.2:n.2866-2047C=
ENST00000448424.6:c.2772C= ENSP00000416738.2:p.Ala924=
ENST00000466629.1:n.226C=
ENST00000634296.1:c.967C=
ENST00000634308.1:c.*107C= ENSP00000489234.1:n.*107C=
ENST00000634620.1:n.3750C=
ENST00000634810.1:n.2351C=
ENST00000634844.1:c.2862C= ENSP00000489398.1:p.Ala954=
ENST00000635406.1:n.352C=
NM_000053.3:c.3006C= NP_000044.2:p.Ala1002=
NM_001005918.2:c.2385C= NP_001005918.1:p.Ala795=
NM_001243182.1:c.2673C= NP_001230111.1:p.Ala891=
XM_005266423.2:c.2910C= XP_005266480.1:p.Ala970=
XM_005266424.3:c.2910C= XP_005266481.1:p.Ala970=
XM_005266427.2:c.2772C= XP_005266484.1:p.Ala924=
XM_005266428.1:c.2754C= XP_005266485.1:p.Ala918=
XM_005266430.3:c.3006C= XP_005266487.1:p.Ala1002=
XM_005266431.2:c.2970C= XP_005266488.1:p.Ala990=
XM_005266432.2:c.2520C= XP_005266489.1:p.Ala840=
XM_006719837.2:c.2910C= XP_006719900.1:p.Ala970=
XM_006719838.1:c.822C= XP_006719901.1:p.Ala274=
XM_006719839.1:c.822C= XP_006719902.1:p.Ala274=
XM_011535117.1:c.2910C= XP_011533419.1:p.Ala970=
XM_011535118.1:c.2871C= XP_011533420.1:p.Ala957=
XM_011535119.1:c.3006C= XP_011533421.1:p.Ala1002=
XM_011535120.1:c.2592C= XP_011533422.1:p.Ala864=
XM_011535121.1:c.2730+3669C= XP_011533423.1:n.2730+3669C=
XM_011535122.1:c.1674C= XP_011533424.1:p.Ala558=
XR_941601.1:n.3225C=
XR_941602.1:n.3225C=
XR_941603.1:n.3225C=
XR_941604.1:n.3225C=
NM_001330578.1:c.2772C= NP_001317507.1:p.Ala924=
NM_001330579.1:c.2754C= NP_001317508.1:p.Ala918=
XM_005266424.4:c.2910C= XP_005266481.1:p.Ala970=
XM_005266430.4:c.3006C= XP_005266487.1:p.Ala1002=
XM_005266431.4:c.2970C= XP_005266488.1:p.Ala990=
XM_006719837.3:c.2910C= XP_006719900.1:p.Ala970=
XM_011535117.3:c.2910C= XP_011533419.1:p.Ala970=
XM_017020627.1:c.2910C= XP_016876116.1:p.Ala970=
NM_000053.4:c.3006C= MANE Select NP_000044.2:p.Ala1002=
NM_001005918.3:c.2385C= NP_001005918.1:p.Ala795=
NM_001330579.2:c.2754C= NP_001317508.1:p.Ala918=
NM_001243182.2:c.2673C= NP_001230111.1:p.Ala891=
NM_001330578.2:c.2772C= NP_001317507.1:p.Ala924=