Canonical Allele Identifier: CA2091542362
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950329G= , CM000675.2:g.51950329G= GRCh38
NC_000013.10:g.52524465G= , CM000675.1:g.52524465G= GRCh37
NC_000013.9:g.51422466G= NCBI36
NG_008806.1:g.66166C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*351C= ENSP00000489512.2:n.*351C=
ENST00000673864.2:c.*1262C= ENSP00000501045.2:n.*1262C=
ENST00000674147.2:c.2032C= ENSP00000500964.2:p.Pro678=
ENST00000242839.10:c.2518C= MANE Select ENSP00000242839.5:p.Pro840=
ENST00000344297.9:c.2032C= ENSP00000342559.5:p.Pro678=
ENST00000400366.6:c.2185C= ENSP00000383217.3:p.Pro729=
ENST00000448424.7:c.2266C= ENSP00000416738.3:p.Pro756=
ENST00000673772.1:c.2284C= ENSP00000501168.1:p.Pro762=
ENST00000674147.1:c.1588C= ENSP00000500964.1:p.Pro530=
ENST00000242839.8:c.2518C= ENSP00000242839.4:p.Pro840=
ENST00000344297.8:c.2032C= ENSP00000342559.5:p.Pro678=
ENST00000400366.5:c.2185C= ENSP00000383217.3:p.Pro729=
ENST00000400370.8:c.1286-168C= ENSP00000383221.3:n.1286-168C=
ENST00000418097.7:c.2518C= ENSP00000393343.2:p.Pro840=
ENST00000448424.6:c.2284C= ENSP00000416738.2:p.Pro762=
ENST00000634296.1:c.479C=
ENST00000634308.1:c.2284C= ENSP00000489234.1:p.Pro762=
ENST00000634620.1:n.3316C=
ENST00000634810.1:n.1863C=
ENST00000634844.1:c.2374C= ENSP00000489398.1:p.Pro792=
ENST00000635406.1:n.212-3851C=
NM_000053.3:c.2518C= NP_000044.2:p.Pro840=
NM_001005918.2:c.2032C= NP_001005918.1:p.Pro678=
NM_001243182.1:c.2185C= NP_001230111.1:p.Pro729=
XM_005266423.2:c.2422C= XP_005266480.1:p.Pro808=
XM_005266424.3:c.2422C= XP_005266481.1:p.Pro808=
XM_005266427.2:c.2284C= XP_005266484.1:p.Pro762=
XM_005266428.1:c.2266C= XP_005266485.1:p.Pro756=
XM_005266430.3:c.2518C= XP_005266487.1:p.Pro840=
XM_005266431.2:c.2482C= XP_005266488.1:p.Pro828=
XM_005266432.2:c.2032C= XP_005266489.1:p.Pro678=
XM_006719837.2:c.2422C= XP_006719900.1:p.Pro808=
XM_006719838.1:c.334C= XP_006719901.1:p.Pro112=
XM_006719839.1:c.334C= XP_006719902.1:p.Pro112=
XM_011535117.1:c.2422C= XP_011533419.1:p.Pro808=
XM_011535118.1:c.2518C= XP_011533420.1:p.Pro840=
XM_011535119.1:c.2518C= XP_011533421.1:p.Pro840=
XM_011535120.1:c.2104C= XP_011533422.1:p.Pro702=
XM_011535121.1:c.2518C= XP_011533423.1:p.Pro840=
XM_011535122.1:c.1186C= XP_011533424.1:p.Pro396=
XR_941601.1:n.2737C=
XR_941602.1:n.2737C=
XR_941603.1:n.2737C=
XR_941604.1:n.2737C=
NM_001330578.1:c.2284C= NP_001317507.1:p.Pro762=
NM_001330579.1:c.2266C= NP_001317508.1:p.Pro756=
XM_005266424.4:c.2422C= XP_005266481.1:p.Pro808=
XM_005266430.4:c.2518C= XP_005266487.1:p.Pro840=
XM_005266431.4:c.2482C= XP_005266488.1:p.Pro828=
XM_006719837.3:c.2422C= XP_006719900.1:p.Pro808=
XM_011535117.3:c.2422C= XP_011533419.1:p.Pro808=
XM_017020627.1:c.2422C= XP_016876116.1:p.Pro808=
NM_000053.4:c.2518C= MANE Select NP_000044.2:p.Pro840=
NM_001005918.3:c.2032C= NP_001005918.1:p.Pro678=
NM_001330579.2:c.2266C= NP_001317508.1:p.Pro756=
NM_001243182.2:c.2185C= NP_001230111.1:p.Pro729=
NM_001330578.2:c.2284C= NP_001317507.1:p.Pro762=