Canonical Allele Identifier: CA388026197

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515259G>C (hg19) ; chr13:g.51941123G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941123G>C , CM000675.2:g.51941123G>C	GRCh38
NC_000013.10:g.52515259G>C , CM000675.1:g.52515259G>C	GRCh37
NC_000013.9:g.51413260G>C	NCBI36
NG_008806.1:g.75372C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1164C>G	ENSP00000489512.2:n.*1164C>G
ENST00000673864.2:c.*2258C>G	ENSP00000501045.2:n.*2258C>G
ENST00000674147.2:c.2893C>G	ENSP00000500964.2:p.His965Asp
ENST00000242839.10:c.3514C>G MANE Select	ENSP00000242839.5:p.His1172Asp
ENST00000344297.9:c.2893C>G	ENSP00000342559.5:p.His965Asp
ENST00000400366.6:c.3181C>G	ENSP00000383217.3:p.His1061Asp
ENST00000448424.7:c.3262C>G	ENSP00000416738.3:p.His1088Asp
ENST00000673772.1:c.3280C>G	ENSP00000501168.1:p.His1094Asp
ENST00000673867.1:n.3653C>G
ENST00000674126.1:n.3877C>G
ENST00000674147.1:c.2449C>G	ENSP00000500964.1:p.His817Asp
ENST00000242839.8:c.3514C>G	ENSP00000242839.4:p.His1172Asp
ENST00000344297.8:c.2893C>G	ENSP00000342559.5:p.His965Asp
ENST00000400366.5:c.3181C>G	ENSP00000383217.3:p.His1061Asp
ENST00000400370.8:c.2224C>G	ENSP00000383221.3:p.His742Asp
ENST00000418097.7:c.3319C>G	ENSP00000393343.2:p.His1107Asp
ENST00000448424.6:c.3280C>G	ENSP00000416738.2:p.His1094Asp
ENST00000634296.1:c.1292C>G
ENST00000634308.1:c.*615C>G	ENSP00000489234.1:n.*615C>G
ENST00000634620.1:n.4258C>G
ENST00000634810.1:n.2859C>G
ENST00000634844.1:c.3370C>G	ENSP00000489398.1:p.His1124Asp
NM_000053.3:c.3514C>G	NP_000044.2:p.His1172Asp
NM_001005918.2:c.2893C>G	NP_001005918.1:p.His965Asp
NM_001243182.1:c.3181C>G	NP_001230111.1:p.His1061Asp
XM_005266423.2:c.3418C>G	XP_005266480.1:p.His1140Asp
XM_005266424.3:c.3418C>G	XP_005266481.1:p.His1140Asp
XM_005266427.2:c.3280C>G	XP_005266484.1:p.His1094Asp
XM_005266428.1:c.3262C>G	XP_005266485.1:p.His1088Asp
XM_005266430.3:c.3514C>G	XP_005266487.1:p.His1172Asp
XM_005266431.2:c.3478C>G	XP_005266488.1:p.His1160Asp
XM_005266432.2:c.3028C>G	XP_005266489.1:p.His1010Asp
XM_006719837.2:c.3418C>G	XP_006719900.1:p.His1140Asp
XM_006719838.1:c.1330C>G	XP_006719901.1:p.His444Asp
XM_006719839.1:c.1147C>G	XP_006719902.1:p.His383Asp
XM_011535117.1:c.3418C>G	XP_011533419.1:p.His1140Asp
XM_011535118.1:c.3379C>G	XP_011533420.1:p.His1127Asp
XM_011535119.1:c.3331C>G	XP_011533421.1:p.His1111Asp
XM_011535120.1:c.3100C>G	XP_011533422.1:p.His1034Asp
XM_011535121.1:c.3001C>G	XP_011533423.1:p.His1001Asp
XM_011535122.1:c.2182C>G	XP_011533424.1:p.His728Asp
XR_941601.1:n.3733C>G
XR_941602.1:n.3733C>G
XR_941603.1:n.3733C>G
XR_941604.1:n.3733C>G
NM_001330578.1:c.3280C>G	NP_001317507.1:p.His1094Asp
NM_001330579.1:c.3262C>G	NP_001317508.1:p.His1088Asp
XM_005266424.4:c.3418C>G	XP_005266481.1:p.His1140Asp
XM_005266430.4:c.3514C>G	XP_005266487.1:p.His1172Asp
XM_005266431.4:c.3478C>G	XP_005266488.1:p.His1160Asp
XM_006719837.3:c.3418C>G	XP_006719900.1:p.His1140Asp
XM_011535117.3:c.3418C>G	XP_011533419.1:p.His1140Asp
XM_017020627.1:c.3418C>G	XP_016876116.1:p.His1140Asp
NM_000053.4:c.3514C>G MANE Select	NP_000044.2:p.His1172Asp
NM_001005918.3:c.2893C>G	NP_001005918.1:p.His965Asp
NM_001330579.2:c.3262C>G	NP_001317508.1:p.His1088Asp
NM_001243182.2:c.3181C>G	NP_001230111.1:p.His1061Asp
NM_001330578.2:c.3280C>G	NP_001317507.1:p.His1094Asp