Canonical Allele Identifier: CA388026238

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51941126-C-T
• MyVariant Identifiers: chr13:g.52515262C>T (hg19) ; chr13:g.51941126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941126C>T , CM000675.2:g.51941126C>T	GRCh38
NC_000013.10:g.52515262C>T , CM000675.1:g.52515262C>T	GRCh37
NC_000013.9:g.51413263C>T	NCBI36
NG_008806.1:g.75369G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1161G>A	ENSP00000489512.2:n.*1161G>A
ENST00000673864.2:c.*2255G>A	ENSP00000501045.2:n.*2255G>A
ENST00000674147.2:c.2890G>A	ENSP00000500964.2:p.Asp964Asn
ENST00000242839.10:c.3511G>A MANE Select	ENSP00000242839.5:p.Asp1171Asn
ENST00000344297.9:c.2890G>A	ENSP00000342559.5:p.Asp964Asn
ENST00000400366.6:c.3178G>A	ENSP00000383217.3:p.Asp1060Asn
ENST00000448424.7:c.3259G>A	ENSP00000416738.3:p.Asp1087Asn
ENST00000673772.1:c.3277G>A	ENSP00000501168.1:p.Asp1093Asn
ENST00000673867.1:n.3650G>A
ENST00000674126.1:n.3874G>A
ENST00000674147.1:c.2446G>A	ENSP00000500964.1:p.Asp816Asn
ENST00000242839.8:c.3511G>A	ENSP00000242839.4:p.Asp1171Asn
ENST00000344297.8:c.2890G>A	ENSP00000342559.5:p.Asp964Asn
ENST00000400366.5:c.3178G>A	ENSP00000383217.3:p.Asp1060Asn
ENST00000400370.8:c.2221G>A	ENSP00000383221.3:p.Asp741Asn
ENST00000418097.7:c.3316G>A	ENSP00000393343.2:p.Asp1106Asn
ENST00000448424.6:c.3277G>A	ENSP00000416738.2:p.Asp1093Asn
ENST00000634296.1:c.1289G>A
ENST00000634308.1:c.*612G>A	ENSP00000489234.1:n.*612G>A
ENST00000634620.1:n.4255G>A
ENST00000634810.1:n.2856G>A
ENST00000634844.1:c.3367G>A	ENSP00000489398.1:p.Asp1123Asn
NM_000053.3:c.3511G>A	NP_000044.2:p.Asp1171Asn
NM_001005918.2:c.2890G>A	NP_001005918.1:p.Asp964Asn
NM_001243182.1:c.3178G>A	NP_001230111.1:p.Asp1060Asn
XM_005266423.2:c.3415G>A	XP_005266480.1:p.Asp1139Asn
XM_005266424.3:c.3415G>A	XP_005266481.1:p.Asp1139Asn
XM_005266427.2:c.3277G>A	XP_005266484.1:p.Asp1093Asn
XM_005266428.1:c.3259G>A	XP_005266485.1:p.Asp1087Asn
XM_005266430.3:c.3511G>A	XP_005266487.1:p.Asp1171Asn
XM_005266431.2:c.3475G>A	XP_005266488.1:p.Asp1159Asn
XM_005266432.2:c.3025G>A	XP_005266489.1:p.Asp1009Asn
XM_006719837.2:c.3415G>A	XP_006719900.1:p.Asp1139Asn
XM_006719838.1:c.1327G>A	XP_006719901.1:p.Asp443Asn
XM_006719839.1:c.1144G>A	XP_006719902.1:p.Asp382Asn
XM_011535117.1:c.3415G>A	XP_011533419.1:p.Asp1139Asn
XM_011535118.1:c.3376G>A	XP_011533420.1:p.Asp1126Asn
XM_011535119.1:c.3328G>A	XP_011533421.1:p.Asp1110Asn
XM_011535120.1:c.3097G>A	XP_011533422.1:p.Asp1033Asn
XM_011535121.1:c.2998G>A	XP_011533423.1:p.Asp1000Asn
XM_011535122.1:c.2179G>A	XP_011533424.1:p.Asp727Asn
XR_941601.1:n.3730G>A
XR_941602.1:n.3730G>A
XR_941603.1:n.3730G>A
XR_941604.1:n.3730G>A
NM_001330578.1:c.3277G>A	NP_001317507.1:p.Asp1093Asn
NM_001330579.1:c.3259G>A	NP_001317508.1:p.Asp1087Asn
XM_005266424.4:c.3415G>A	XP_005266481.1:p.Asp1139Asn
XM_005266430.4:c.3511G>A	XP_005266487.1:p.Asp1171Asn
XM_005266431.4:c.3475G>A	XP_005266488.1:p.Asp1159Asn
XM_006719837.3:c.3415G>A	XP_006719900.1:p.Asp1139Asn
XM_011535117.3:c.3415G>A	XP_011533419.1:p.Asp1139Asn
XM_017020627.1:c.3415G>A	XP_016876116.1:p.Asp1139Asn
NM_000053.4:c.3511G>A MANE Select	NP_000044.2:p.Asp1171Asn
NM_001005918.3:c.2890G>A	NP_001005918.1:p.Asp964Asn
NM_001330579.2:c.3259G>A	NP_001317508.1:p.Asp1087Asn
NM_001243182.2:c.3178G>A	NP_001230111.1:p.Asp1060Asn
NM_001330578.2:c.3277G>A	NP_001317507.1:p.Asp1093Asn