Canonical Allele Identifier: CA388029898

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518284T>G (hg19) ; chr13:g.51944148T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944148T>G , CM000675.2:g.51944148T>G	GRCh38
NC_000013.10:g.52518284T>G , CM000675.1:g.52518284T>G	GRCh37
NC_000013.9:g.51416285T>G	NCBI36
NG_008806.1:g.72347A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*894-1594A>C	ENSP00000489512.2:n.*894-1594A>C
ENST00000673864.2:c.*1948A>C	ENSP00000501045.2:n.*1948A>C
ENST00000674147.2:c.2583A>C	ENSP00000500964.2:p.Glu861Asp
ENST00000242839.10:c.3204A>C MANE Select	ENSP00000242839.5:p.Glu1068Asp
ENST00000344297.9:c.2583A>C	ENSP00000342559.5:p.Glu861Asp
ENST00000400366.6:c.2871A>C	ENSP00000383217.3:p.Glu957Asp
ENST00000448424.7:c.2952A>C	ENSP00000416738.3:p.Glu984Asp
ENST00000673772.1:c.2970A>C	ENSP00000501168.1:p.Glu990Asp
ENST00000673867.1:n.3343A>C
ENST00000674126.1:n.3567A>C
ENST00000674147.1:c.2139A>C	ENSP00000500964.1:p.Glu713Asp
ENST00000242839.8:c.3204A>C	ENSP00000242839.4:p.Glu1068Asp
ENST00000344297.8:c.2583A>C	ENSP00000342559.5:p.Glu861Asp
ENST00000400366.5:c.2871A>C	ENSP00000383217.3:p.Glu957Asp
ENST00000400370.8:c.1914A>C	ENSP00000383221.3:p.Glu638Asp
ENST00000418097.7:c.3009A>C	ENSP00000393343.2:p.Glu1003Asp
ENST00000448424.6:c.2970A>C	ENSP00000416738.2:p.Glu990Asp
ENST00000466629.1:n.424A>C
ENST00000634296.1:c.1022-1594A>C
ENST00000634308.1:c.*305A>C	ENSP00000489234.1:n.*305A>C
ENST00000634620.1:n.3948A>C
ENST00000634810.1:n.2549A>C
ENST00000634844.1:c.3060A>C	ENSP00000489398.1:p.Glu1020Asp
NM_000053.3:c.3204A>C	NP_000044.2:p.Glu1068Asp
NM_001005918.2:c.2583A>C	NP_001005918.1:p.Glu861Asp
NM_001243182.1:c.2871A>C	NP_001230111.1:p.Glu957Asp
XM_005266423.2:c.3108A>C	XP_005266480.1:p.Glu1036Asp
XM_005266424.3:c.3108A>C	XP_005266481.1:p.Glu1036Asp
XM_005266427.2:c.2970A>C	XP_005266484.1:p.Glu990Asp
XM_005266428.1:c.2952A>C	XP_005266485.1:p.Glu984Asp
XM_005266430.3:c.3204A>C	XP_005266487.1:p.Glu1068Asp
XM_005266431.2:c.3168A>C	XP_005266488.1:p.Glu1056Asp
XM_005266432.2:c.2718A>C	XP_005266489.1:p.Glu906Asp
XM_006719837.2:c.3108A>C	XP_006719900.1:p.Glu1036Asp
XM_006719838.1:c.1020A>C	XP_006719901.1:p.Glu340Asp
XM_006719839.1:c.877-1594A>C	XP_006719902.1:n.877-1594A>C
XM_011535117.1:c.3108A>C	XP_011533419.1:p.Glu1036Asp
XM_011535118.1:c.3069A>C	XP_011533420.1:p.Glu1023Asp
XM_011535119.1:c.3061-1594A>C	XP_011533421.1:n.3061-1594A>C
XM_011535120.1:c.2790A>C	XP_011533422.1:p.Glu930Asp
XM_011535121.1:c.2731-1594A>C	XP_011533423.1:n.2731-1594A>C
XM_011535122.1:c.1872A>C	XP_011533424.1:p.Glu624Asp
XR_941601.1:n.3423A>C
XR_941602.1:n.3423A>C
XR_941603.1:n.3423A>C
XR_941604.1:n.3423A>C
NM_001330578.1:c.2970A>C	NP_001317507.1:p.Glu990Asp
NM_001330579.1:c.2952A>C	NP_001317508.1:p.Glu984Asp
XM_005266424.4:c.3108A>C	XP_005266481.1:p.Glu1036Asp
XM_005266430.4:c.3204A>C	XP_005266487.1:p.Glu1068Asp
XM_005266431.4:c.3168A>C	XP_005266488.1:p.Glu1056Asp
XM_006719837.3:c.3108A>C	XP_006719900.1:p.Glu1036Asp
XM_011535117.3:c.3108A>C	XP_011533419.1:p.Glu1036Asp
XM_017020627.1:c.3108A>C	XP_016876116.1:p.Glu1036Asp
NM_000053.4:c.3204A>C MANE Select	NP_000044.2:p.Glu1068Asp
NM_001005918.3:c.2583A>C	NP_001005918.1:p.Glu861Asp
NM_001330579.2:c.2952A>C	NP_001317508.1:p.Glu984Asp
NM_001243182.2:c.2871A>C	NP_001230111.1:p.Glu957Asp
NM_001330578.2:c.2970A>C	NP_001317507.1:p.Glu990Asp