Canonical Allele Identifier: CA2091553331
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51937293C= , CM000675.2:g.51937293C= GRCh38
NC_000013.10:g.52511429C= , CM000675.1:g.52511429C= GRCh37
NC_000013.9:g.51409430C= NCBI36
NG_008806.1:g.79202G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1654G= ENSP00000489512.2:n.*1654G=
ENST00000673864.2:c.*2748G= ENSP00000501045.2:n.*2748G=
ENST00000674147.2:c.3383G= ENSP00000500964.2:p.Gly1128=
ENST00000242839.10:c.4004G= MANE Select ENSP00000242839.5:p.Gly1335=
ENST00000344297.9:c.3383G= ENSP00000342559.5:p.Gly1128=
ENST00000400366.6:c.3671G= ENSP00000383217.3:p.Gly1224=
ENST00000448424.7:c.3752G= ENSP00000416738.3:p.Gly1251=
ENST00000673696.1:n.1327G=
ENST00000673772.1:c.3770G= ENSP00000501168.1:p.Gly1257=
ENST00000673867.1:n.4143G=
ENST00000673923.1:n.870G=
ENST00000674147.1:c.2939G= ENSP00000500964.1:p.Gly980=
ENST00000242839.8:c.4004G= ENSP00000242839.4:p.Gly1335=
ENST00000344297.8:c.3383G= ENSP00000342559.5:p.Gly1128=
ENST00000400366.5:c.3671G= ENSP00000383217.3:p.Gly1224=
ENST00000400370.8:c.2714G= ENSP00000383221.3:p.Gly905=
ENST00000418097.7:c.3809G= ENSP00000393343.2:p.Gly1270=
ENST00000448424.6:c.3770G= ENSP00000416738.2:p.Gly1257=
ENST00000634296.1:c.1782G=
ENST00000634308.1:c.*1105G= ENSP00000489234.1:n.*1105G=
ENST00000634620.1:n.4748G=
ENST00000634810.1:n.3349G=
ENST00000634844.1:c.3860G= ENSP00000489398.1:p.Gly1287=
NM_000053.3:c.4004G= NP_000044.2:p.Gly1335=
NM_001005918.2:c.3383G= NP_001005918.1:p.Gly1128=
NM_001243182.1:c.3671G= NP_001230111.1:p.Gly1224=
XM_005266423.2:c.3908G= XP_005266480.1:p.Gly1303=
XM_005266424.3:c.3908G= XP_005266481.1:p.Gly1303=
XM_005266427.2:c.3770G= XP_005266484.1:p.Gly1257=
XM_005266428.1:c.3752G= XP_005266485.1:p.Gly1251=
XM_005266430.3:c.4004G= XP_005266487.1:p.Gly1335=
XM_005266431.2:c.3968G= XP_005266488.1:p.Gly1323=
XM_005266432.2:c.3518G= XP_005266489.1:p.Gly1173=
XM_006719837.2:c.3908G= XP_006719900.1:p.Gly1303=
XM_006719838.1:c.1820G= XP_006719901.1:p.Gly607=
XM_006719839.1:c.1637G= XP_006719902.1:p.Gly546=
XM_011535117.1:c.3908G= XP_011533419.1:p.Gly1303=
XM_011535118.1:c.3869G= XP_011533420.1:p.Gly1290=
XM_011535119.1:c.3821G= XP_011533421.1:p.Gly1274=
XM_011535120.1:c.3590G= XP_011533422.1:p.Gly1197=
XM_011535121.1:c.3491G= XP_011533423.1:p.Gly1164=
XM_011535122.1:c.2672G= XP_011533424.1:p.Gly891=
XR_941601.1:n.4223G=
XR_941602.1:n.4223G=
XR_941603.1:n.4223G=
XR_941604.1:n.4223G=
NM_001330578.1:c.3770G= NP_001317507.1:p.Gly1257=
NM_001330579.1:c.3752G= NP_001317508.1:p.Gly1251=
XM_005266424.4:c.3908G= XP_005266481.1:p.Gly1303=
XM_005266430.4:c.4004G= XP_005266487.1:p.Gly1335=
XM_005266431.4:c.3968G= XP_005266488.1:p.Gly1323=
XM_006719837.3:c.3908G= XP_006719900.1:p.Gly1303=
XM_011535117.3:c.3908G= XP_011533419.1:p.Gly1303=
XM_017020627.1:c.3908G= XP_016876116.1:p.Gly1303=
NM_000053.4:c.4004G= MANE Select NP_000044.2:p.Gly1335=
NM_001005918.3:c.3383G= NP_001005918.1:p.Gly1128=
NM_001330579.2:c.3752G= NP_001317508.1:p.Gly1251=
NM_001243182.2:c.3671G= NP_001230111.1:p.Gly1224=
NM_001330578.2:c.3770G= NP_001317507.1:p.Gly1257=