Canonical Allele Identifier: CA6988687

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 312380
• ClinVar RCV Id: RCV003151766
• dbSNP Id: rs757549770
• ExAC: 13:52515351 G / C
• gnomAD v2: 13-52515351-G-C
• gnomAD v3: 13-51941215-G-C
• gnomAD v4: 13-51941215-G-C
• MyVariant Identifiers: chr13:g.52515351G>C (hg19) ; chr13:g.51941215G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941215G>C , CM000675.2:g.51941215G>C	GRCh38
NC_000013.10:g.52515351G>C , CM000675.1:g.52515351G>C	GRCh37
NC_000013.9:g.51413352G>C	NCBI36
NG_008806.1:g.75280C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1072C>G	ENSP00000489512.2:n.*1072C>G
ENST00000673864.2:c.*2166C>G	ENSP00000501045.2:n.*2166C>G
ENST00000674147.2:c.2801C>G	ENSP00000500964.2:p.Pro934Arg
ENST00000242839.10:c.3422C>G MANE Select	ENSP00000242839.5:p.Pro1141Arg
ENST00000344297.9:c.2801C>G	ENSP00000342559.5:p.Pro934Arg
ENST00000400366.6:c.3089C>G	ENSP00000383217.3:p.Pro1030Arg
ENST00000448424.7:c.3170C>G	ENSP00000416738.3:p.Pro1057Arg
ENST00000673772.1:c.3188C>G	ENSP00000501168.1:p.Pro1063Arg
ENST00000673867.1:n.3561C>G
ENST00000674126.1:n.3785C>G
ENST00000674147.1:c.2357C>G	ENSP00000500964.1:p.Pro786Arg
ENST00000242839.8:c.3422C>G	ENSP00000242839.4:p.Pro1141Arg
ENST00000344297.8:c.2801C>G	ENSP00000342559.5:p.Pro934Arg
ENST00000400366.5:c.3089C>G	ENSP00000383217.3:p.Pro1030Arg
ENST00000400370.8:c.2132C>G	ENSP00000383221.3:p.Pro711Arg
ENST00000418097.7:c.3227C>G	ENSP00000393343.2:p.Pro1076Arg
ENST00000448424.6:c.3188C>G	ENSP00000416738.2:p.Pro1063Arg
ENST00000634296.1:c.1200C>G
ENST00000634308.1:c.*523C>G	ENSP00000489234.1:n.*523C>G
ENST00000634620.1:n.4166C>G
ENST00000634810.1:n.2767C>G
ENST00000634844.1:c.3278C>G	ENSP00000489398.1:p.Pro1093Arg
NM_000053.3:c.3422C>G	NP_000044.2:p.Pro1141Arg
NM_001005918.2:c.2801C>G	NP_001005918.1:p.Pro934Arg
NM_001243182.1:c.3089C>G	NP_001230111.1:p.Pro1030Arg
XM_005266423.2:c.3326C>G	XP_005266480.1:p.Pro1109Arg
XM_005266424.3:c.3326C>G	XP_005266481.1:p.Pro1109Arg
XM_005266427.2:c.3188C>G	XP_005266484.1:p.Pro1063Arg
XM_005266428.1:c.3170C>G	XP_005266485.1:p.Pro1057Arg
XM_005266430.3:c.3422C>G	XP_005266487.1:p.Pro1141Arg
XM_005266431.2:c.3386C>G	XP_005266488.1:p.Pro1129Arg
XM_005266432.2:c.2936C>G	XP_005266489.1:p.Pro979Arg
XM_006719837.2:c.3326C>G	XP_006719900.1:p.Pro1109Arg
XM_006719838.1:c.1238C>G	XP_006719901.1:p.Pro413Arg
XM_006719839.1:c.1055C>G	XP_006719902.1:p.Pro352Arg
XM_011535117.1:c.3326C>G	XP_011533419.1:p.Pro1109Arg
XM_011535118.1:c.3287C>G	XP_011533420.1:p.Pro1096Arg
XM_011535119.1:c.3239C>G	XP_011533421.1:p.Pro1080Arg
XM_011535120.1:c.3008C>G	XP_011533422.1:p.Pro1003Arg
XM_011535121.1:c.2909C>G	XP_011533423.1:p.Pro970Arg
XM_011535122.1:c.2090C>G	XP_011533424.1:p.Pro697Arg
XR_941601.1:n.3641C>G
XR_941602.1:n.3641C>G
XR_941603.1:n.3641C>G
XR_941604.1:n.3641C>G
NM_001330578.1:c.3188C>G	NP_001317507.1:p.Pro1063Arg
NM_001330579.1:c.3170C>G	NP_001317508.1:p.Pro1057Arg
XM_005266424.4:c.3326C>G	XP_005266481.1:p.Pro1109Arg
XM_005266430.4:c.3422C>G	XP_005266487.1:p.Pro1141Arg
XM_005266431.4:c.3386C>G	XP_005266488.1:p.Pro1129Arg
XM_006719837.3:c.3326C>G	XP_006719900.1:p.Pro1109Arg
XM_011535117.3:c.3326C>G	XP_011533419.1:p.Pro1109Arg
XM_017020627.1:c.3326C>G	XP_016876116.1:p.Pro1109Arg
NM_000053.4:c.3422C>G MANE Select	NP_000044.2:p.Pro1141Arg
NM_001005918.3:c.2801C>G	NP_001005918.1:p.Pro934Arg
NM_001330579.2:c.3170C>G	NP_001317508.1:p.Pro1057Arg
NM_001243182.2:c.3089C>G	NP_001230111.1:p.Pro1030Arg
NM_001330578.2:c.3188C>G	NP_001317507.1:p.Pro1063Arg