Canonical Allele Identifier: CA2091556789
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939112C= , CM000675.2:g.51939112C= GRCh38
NC_000013.10:g.52513248C= , CM000675.1:g.52513248C= GRCh37
NC_000013.9:g.51411249C= NCBI36
NG_008806.1:g.77383G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1288G= ENSP00000489512.2:n.*1288G=
ENST00000673864.2:c.*2382G= ENSP00000501045.2:n.*2382G=
ENST00000674147.2:c.3017G= ENSP00000500964.2:p.Gly1006=
ENST00000242839.10:c.3638G= MANE Select ENSP00000242839.5:p.Gly1213=
ENST00000344297.9:c.3017G= ENSP00000342559.5:p.Gly1006=
ENST00000400366.6:c.3305G= ENSP00000383217.3:p.Gly1102=
ENST00000448424.7:c.3386G= ENSP00000416738.3:p.Gly1129=
ENST00000673696.1:n.879G=
ENST00000673772.1:c.3404G= ENSP00000501168.1:p.Gly1135=
ENST00000673867.1:n.3777G=
ENST00000673923.1:n.504G=
ENST00000674147.1:c.2573G= ENSP00000500964.1:p.Gly858=
ENST00000242839.8:c.3638G= ENSP00000242839.4:p.Gly1213=
ENST00000344297.8:c.3017G= ENSP00000342559.5:p.Gly1006=
ENST00000400366.5:c.3305G= ENSP00000383217.3:p.Gly1102=
ENST00000400370.8:c.2348G= ENSP00000383221.3:p.Gly783=
ENST00000418097.7:c.3443G= ENSP00000393343.2:p.Gly1148=
ENST00000448424.6:c.3404G= ENSP00000416738.2:p.Gly1135=
ENST00000634296.1:c.1416G=
ENST00000634308.1:c.*739G= ENSP00000489234.1:n.*739G=
ENST00000634620.1:n.4382G=
ENST00000634810.1:n.2983G=
ENST00000634844.1:c.3494G= ENSP00000489398.1:p.Gly1165=
NM_000053.3:c.3638G= NP_000044.2:p.Gly1213=
NM_001005918.2:c.3017G= NP_001005918.1:p.Gly1006=
NM_001243182.1:c.3305G= NP_001230111.1:p.Gly1102=
XM_005266423.2:c.3542G= XP_005266480.1:p.Gly1181=
XM_005266424.3:c.3542G= XP_005266481.1:p.Gly1181=
XM_005266427.2:c.3404G= XP_005266484.1:p.Gly1135=
XM_005266428.1:c.3386G= XP_005266485.1:p.Gly1129=
XM_005266430.3:c.3638G= XP_005266487.1:p.Gly1213=
XM_005266431.2:c.3602G= XP_005266488.1:p.Gly1201=
XM_005266432.2:c.3152G= XP_005266489.1:p.Gly1051=
XM_006719837.2:c.3542G= XP_006719900.1:p.Gly1181=
XM_006719838.1:c.1454G= XP_006719901.1:p.Gly485=
XM_006719839.1:c.1271G= XP_006719902.1:p.Gly424=
XM_011535117.1:c.3542G= XP_011533419.1:p.Gly1181=
XM_011535118.1:c.3503G= XP_011533420.1:p.Gly1168=
XM_011535119.1:c.3455G= XP_011533421.1:p.Gly1152=
XM_011535120.1:c.3224G= XP_011533422.1:p.Gly1075=
XM_011535121.1:c.3125G= XP_011533423.1:p.Gly1042=
XM_011535122.1:c.2306G= XP_011533424.1:p.Gly769=
XR_941601.1:n.3857G=
XR_941602.1:n.3857G=
XR_941603.1:n.3857G=
XR_941604.1:n.3857G=
NM_001330578.1:c.3404G= NP_001317507.1:p.Gly1135=
NM_001330579.1:c.3386G= NP_001317508.1:p.Gly1129=
XM_005266424.4:c.3542G= XP_005266481.1:p.Gly1181=
XM_005266430.4:c.3638G= XP_005266487.1:p.Gly1213=
XM_005266431.4:c.3602G= XP_005266488.1:p.Gly1201=
XM_006719837.3:c.3542G= XP_006719900.1:p.Gly1181=
XM_011535117.3:c.3542G= XP_011533419.1:p.Gly1181=
XM_017020627.1:c.3542G= XP_016876116.1:p.Gly1181=
NM_000053.4:c.3638G= MANE Select NP_000044.2:p.Gly1213=
NM_001005918.3:c.3017G= NP_001005918.1:p.Gly1006=
NM_001330579.2:c.3386G= NP_001317508.1:p.Gly1129=
NM_001243182.2:c.3305G= NP_001230111.1:p.Gly1102=
NM_001330578.2:c.3404G= NP_001317507.1:p.Gly1135=