Canonical Allele Identifier: CA388033637

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51949732G>T , CM000675.2:g.51949732G>T	GRCh38
NC_000013.10:g.52523868G>T , CM000675.1:g.52523868G>T	GRCh37
NC_000013.9:g.51421869G>T	NCBI36
NG_008806.1:g.66763C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000053.4:c.2795C>A MANE Select	NP_000044.2:p.Ser932Ter
ENST00000242839.10:c.2795C>A MANE Select	ENSP00000242839.5:p.Ser932Ter
NM_000053.3:c.2795C>A	NP_000044.2:p.Ser932Ter
NM_001005918.2:c.2244+275C>A	NP_001005918.1:n.2244+275C>A
NM_001005918.3:c.2244+275C>A	NP_001005918.1:n.2244+275C>A
NM_001243182.1:c.2462C>A	NP_001230111.1:p.Ser821Ter
NM_001243182.2:c.2462C>A	NP_001230111.1:p.Ser821Ter
NM_001330578.1:c.2561C>A	NP_001317507.1:p.Ser854Ter
NM_001330578.2:c.2561C>A	NP_001317507.1:p.Ser854Ter
NM_001330579.1:c.2543C>A	NP_001317508.1:p.Ser848Ter
NM_001330579.2:c.2543C>A	NP_001317508.1:p.Ser848Ter
ENST00000242839.8:c.2795C>A	ENSP00000242839.4:p.Ser932Ter
ENST00000344297.8:c.2244+275C>A	ENSP00000342559.5:n.2244+275C>A
ENST00000344297.9:c.2244+275C>A	ENSP00000342559.5:n.2244+275C>A
ENST00000400366.5:c.2462C>A	ENSP00000383217.3:p.Ser821Ter
ENST00000400366.6:c.2462C>A	ENSP00000383217.3:p.Ser821Ter
ENST00000400370.8:c.1505C>A	ENSP00000383221.3:p.Ser502Ter
ENST00000418097.7:c.2795C>A	ENSP00000393343.2:p.Ser932Ter
ENST00000448424.6:c.2561C>A	ENSP00000416738.2:p.Ser854Ter
ENST00000448424.7:c.2543C>A	ENSP00000416738.3:p.Ser848Ter
ENST00000634296.1:c.756C>A
ENST00000634296.2:c.*628C>A	ENSP00000489512.2:n.*628C>A
ENST00000634308.1:c.2561C>A	ENSP00000489234.1:p.Ser854Ter
ENST00000634620.1:n.3593C>A
ENST00000634810.1:n.2140C>A
ENST00000634844.1:c.2651C>A	ENSP00000489398.1:p.Ser884Ter
ENST00000635406.1:n.212-3254C>A
ENST00000673772.1:c.2561C>A	ENSP00000501168.1:p.Ser854Ter
ENST00000673864.2:c.*1539C>A	ENSP00000501045.2:n.*1539C>A
ENST00000674147.1:c.1800+275C>A	ENSP00000500964.1:n.1800+275C>A
ENST00000674147.2:c.2244+275C>A	ENSP00000500964.2:n.2244+275C>A
XM_005266423.2:c.2699C>A	XP_005266480.1:p.Ser900Ter
XM_005266424.3:c.2699C>A	XP_005266481.1:p.Ser900Ter
XM_005266424.4:c.2699C>A	XP_005266481.1:p.Ser900Ter
XM_005266427.2:c.2561C>A	XP_005266484.1:p.Ser854Ter
XM_005266428.1:c.2543C>A	XP_005266485.1:p.Ser848Ter
XM_005266430.3:c.2795C>A	XP_005266487.1:p.Ser932Ter
XM_005266430.4:c.2795C>A	XP_005266487.1:p.Ser932Ter
XM_005266431.2:c.2759C>A	XP_005266488.1:p.Ser920Ter
XM_005266431.4:c.2759C>A	XP_005266488.1:p.Ser920Ter
XM_005266432.2:c.2309C>A	XP_005266489.1:p.Ser770Ter
XM_006719837.2:c.2699C>A	XP_006719900.1:p.Ser900Ter
XM_006719837.3:c.2699C>A	XP_006719900.1:p.Ser900Ter
XM_006719838.1:c.611C>A	XP_006719901.1:p.Ser204Ter
XM_006719839.1:c.611C>A	XP_006719902.1:p.Ser204Ter
XM_011535117.1:c.2699C>A	XP_011533419.1:p.Ser900Ter
XM_011535117.3:c.2699C>A	XP_011533419.1:p.Ser900Ter
XM_011535118.1:c.2730+275C>A	XP_011533420.1:n.2730+275C>A
XM_011535119.1:c.2795C>A	XP_011533421.1:p.Ser932Ter
XM_011535120.1:c.2381C>A	XP_011533422.1:p.Ser794Ter
XM_011535121.1:c.2730+275C>A	XP_011533423.1:n.2730+275C>A
XM_011535122.1:c.1463C>A	XP_011533424.1:p.Ser488Ter
XM_017020627.1:c.2699C>A	XP_016876116.1:p.Ser900Ter
XR_941601.1:n.3014C>A
XR_941602.1:n.3014C>A
XR_941603.1:n.3014C>A
XR_941604.1:n.3014C>A