Canonical Allele Identifier: CA2091556964
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939186G= , CM000675.2:g.51939186G= GRCh38
NC_000013.10:g.52513322G= , CM000675.1:g.52513322G= GRCh37
NC_000013.9:g.51411323G= NCBI36
NG_008806.1:g.77309C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1214C= ENSP00000489512.2:n.*1214C=
ENST00000673864.2:c.*2308C= ENSP00000501045.2:n.*2308C=
ENST00000674147.2:c.2943C= ENSP00000500964.2:p.Leu981=
ENST00000242839.10:c.3564C= MANE Select ENSP00000242839.5:p.Leu1188=
ENST00000344297.9:c.2943C= ENSP00000342559.5:p.Leu981=
ENST00000400366.6:c.3231C= ENSP00000383217.3:p.Leu1077=
ENST00000448424.7:c.3312C= ENSP00000416738.3:p.Leu1104=
ENST00000673696.1:n.805C=
ENST00000673772.1:c.3330C= ENSP00000501168.1:p.Leu1110=
ENST00000673867.1:n.3703C=
ENST00000673923.1:n.430C=
ENST00000674147.1:c.2499C= ENSP00000500964.1:p.Leu833=
ENST00000242839.8:c.3564C= ENSP00000242839.4:p.Leu1188=
ENST00000344297.8:c.2943C= ENSP00000342559.5:p.Leu981=
ENST00000400366.5:c.3231C= ENSP00000383217.3:p.Leu1077=
ENST00000400370.8:c.2274C= ENSP00000383221.3:p.Leu758=
ENST00000418097.7:c.3369C= ENSP00000393343.2:p.Leu1123=
ENST00000448424.6:c.3330C= ENSP00000416738.2:p.Leu1110=
ENST00000634296.1:c.1342C=
ENST00000634308.1:c.*665C= ENSP00000489234.1:n.*665C=
ENST00000634620.1:n.4308C=
ENST00000634810.1:n.2909C=
ENST00000634844.1:c.3420C= ENSP00000489398.1:p.Leu1140=
NM_000053.3:c.3564C= NP_000044.2:p.Leu1188=
NM_001005918.2:c.2943C= NP_001005918.1:p.Leu981=
NM_001243182.1:c.3231C= NP_001230111.1:p.Leu1077=
XM_005266423.2:c.3468C= XP_005266480.1:p.Leu1156=
XM_005266424.3:c.3468C= XP_005266481.1:p.Leu1156=
XM_005266427.2:c.3330C= XP_005266484.1:p.Leu1110=
XM_005266428.1:c.3312C= XP_005266485.1:p.Leu1104=
XM_005266430.3:c.3564C= XP_005266487.1:p.Leu1188=
XM_005266431.2:c.3528C= XP_005266488.1:p.Leu1176=
XM_005266432.2:c.3078C= XP_005266489.1:p.Leu1026=
XM_006719837.2:c.3468C= XP_006719900.1:p.Leu1156=
XM_006719838.1:c.1380C= XP_006719901.1:p.Leu460=
XM_006719839.1:c.1197C= XP_006719902.1:p.Leu399=
XM_011535117.1:c.3468C= XP_011533419.1:p.Leu1156=
XM_011535118.1:c.3429C= XP_011533420.1:p.Leu1143=
XM_011535119.1:c.3381C= XP_011533421.1:p.Leu1127=
XM_011535120.1:c.3150C= XP_011533422.1:p.Leu1050=
XM_011535121.1:c.3051C= XP_011533423.1:p.Leu1017=
XM_011535122.1:c.2232C= XP_011533424.1:p.Leu744=
XR_941601.1:n.3783C=
XR_941602.1:n.3783C=
XR_941603.1:n.3783C=
XR_941604.1:n.3783C=
NM_001330578.1:c.3330C= NP_001317507.1:p.Leu1110=
NM_001330579.1:c.3312C= NP_001317508.1:p.Leu1104=
XM_005266424.4:c.3468C= XP_005266481.1:p.Leu1156=
XM_005266430.4:c.3564C= XP_005266487.1:p.Leu1188=
XM_005266431.4:c.3528C= XP_005266488.1:p.Leu1176=
XM_006719837.3:c.3468C= XP_006719900.1:p.Leu1156=
XM_011535117.3:c.3468C= XP_011533419.1:p.Leu1156=
XM_017020627.1:c.3468C= XP_016876116.1:p.Leu1156=
NM_000053.4:c.3564C= MANE Select NP_000044.2:p.Leu1188=
NM_001005918.3:c.2943C= NP_001005918.1:p.Leu981=
NM_001330579.2:c.3312C= NP_001317508.1:p.Leu1104=
NM_001243182.2:c.3231C= NP_001230111.1:p.Leu1077=
NM_001330578.2:c.3330C= NP_001317507.1:p.Leu1110=