Canonical Allele Identifier: CA388031724

Gene: ATP7B

Linked Data

• dbSNP Id: rs1352113797
• gnomAD v2: 13-52520423-G-C
• gnomAD v4: 13-51946287-G-C
• MyVariant Identifiers: chr13:g.52520423G>C (hg19) ; chr13:g.51946287G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946287G>C , CM000675.2:g.51946287G>C	GRCh38
NC_000013.10:g.52520423G>C , CM000675.1:g.52520423G>C	GRCh37
NC_000013.9:g.51418424G>C	NCBI36
NG_008806.1:g.70208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*890C>G	ENSP00000489512.2:n.*890C>G
ENST00000673864.2:c.*1801C>G	ENSP00000501045.2:n.*1801C>G
ENST00000674147.2:c.2436C>G	ENSP00000500964.2:p.His812Gln
ENST00000242839.10:c.3057C>G MANE Select	ENSP00000242839.5:p.His1019Gln
ENST00000344297.9:c.2436C>G	ENSP00000342559.5:p.His812Gln
ENST00000400366.6:c.2724C>G	ENSP00000383217.3:p.His908Gln
ENST00000448424.7:c.2805C>G	ENSP00000416738.3:p.His935Gln
ENST00000673772.1:c.2823C>G	ENSP00000501168.1:p.His941Gln
ENST00000673867.1:n.1204C>G
ENST00000674126.1:n.3420C>G
ENST00000674147.1:c.1992C>G	ENSP00000500964.1:p.His664Gln
ENST00000242839.8:c.3057C>G	ENSP00000242839.4:p.His1019Gln
ENST00000344297.8:c.2436C>G	ENSP00000342559.5:p.His812Gln
ENST00000400366.5:c.2724C>G	ENSP00000383217.3:p.His908Gln
ENST00000400370.8:c.1767C>G	ENSP00000383221.3:p.His589Gln
ENST00000418097.7:c.2866-1996C>G	ENSP00000393343.2:n.2866-1996C>G
ENST00000448424.6:c.2823C>G	ENSP00000416738.2:p.His941Gln
ENST00000466629.1:n.277C>G
ENST00000634296.1:c.1018C>G
ENST00000634308.1:c.*158C>G	ENSP00000489234.1:n.*158C>G
ENST00000634620.1:n.3801C>G
ENST00000634810.1:n.2402C>G
ENST00000634844.1:c.2913C>G	ENSP00000489398.1:p.His971Gln
ENST00000635406.1:n.403C>G
NM_000053.3:c.3057C>G	NP_000044.2:p.His1019Gln
NM_001005918.2:c.2436C>G	NP_001005918.1:p.His812Gln
NM_001243182.1:c.2724C>G	NP_001230111.1:p.His908Gln
XM_005266423.2:c.2961C>G	XP_005266480.1:p.His987Gln
XM_005266424.3:c.2961C>G	XP_005266481.1:p.His987Gln
XM_005266427.2:c.2823C>G	XP_005266484.1:p.His941Gln
XM_005266428.1:c.2805C>G	XP_005266485.1:p.His935Gln
XM_005266430.3:c.3057C>G	XP_005266487.1:p.His1019Gln
XM_005266431.2:c.3021C>G	XP_005266488.1:p.His1007Gln
XM_005266432.2:c.2571C>G	XP_005266489.1:p.His857Gln
XM_006719837.2:c.2961C>G	XP_006719900.1:p.His987Gln
XM_006719838.1:c.873C>G	XP_006719901.1:p.His291Gln
XM_006719839.1:c.873C>G	XP_006719902.1:p.His291Gln
XM_011535117.1:c.2961C>G	XP_011533419.1:p.His987Gln
XM_011535118.1:c.2922C>G	XP_011533420.1:p.His974Gln
XM_011535119.1:c.3057C>G	XP_011533421.1:p.His1019Gln
XM_011535120.1:c.2643C>G	XP_011533422.1:p.His881Gln
XM_011535121.1:c.2730+3720C>G	XP_011533423.1:n.2730+3720C>G
XM_011535122.1:c.1725C>G	XP_011533424.1:p.His575Gln
XR_941601.1:n.3276C>G
XR_941602.1:n.3276C>G
XR_941603.1:n.3276C>G
XR_941604.1:n.3276C>G
NM_001330578.1:c.2823C>G	NP_001317507.1:p.His941Gln
NM_001330579.1:c.2805C>G	NP_001317508.1:p.His935Gln
XM_005266424.4:c.2961C>G	XP_005266481.1:p.His987Gln
XM_005266430.4:c.3057C>G	XP_005266487.1:p.His1019Gln
XM_005266431.4:c.3021C>G	XP_005266488.1:p.His1007Gln
XM_006719837.3:c.2961C>G	XP_006719900.1:p.His987Gln
XM_011535117.3:c.2961C>G	XP_011533419.1:p.His987Gln
XM_017020627.1:c.2961C>G	XP_016876116.1:p.His987Gln
NM_000053.4:c.3057C>G MANE Select	NP_000044.2:p.His1019Gln
NM_001005918.3:c.2436C>G	NP_001005918.1:p.His812Gln
NM_001330579.2:c.2805C>G	NP_001317508.1:p.His935Gln
NM_001243182.2:c.2724C>G	NP_001230111.1:p.His908Gln
NM_001330578.2:c.2823C>G	NP_001317507.1:p.His941Gln