Canonical Allele Identifier: CA609970386

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 1963031
• ClinVar RCV Id: RCV002710857
• dbSNP Id: rs1566582661
• gnomAD v2: 13-52544892-T-TA
• gnomAD v4: 13-51970756-T-TA
• MyVariant Identifiers: chr13:g.52544892_52544893insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51970760dup , CM000675.2:g.51970760dup	GRCh38
NC_000013.10:g.52544896dup , CM000675.1:g.52544896dup	GRCh37
NC_000013.9:g.51442897dup	NCBI36
NG_008806.1:g.45738dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.1286-8dup	ENSP00000489512.2:n.1286-8dup
ENST00000673864.2:c.*30-8dup	ENSP00000501045.2:n.*30-8dup
ENST00000674147.2:c.1286-8dup	ENSP00000500964.2:n.1286-8dup
ENST00000242839.10:c.1286-8dup MANE Select	ENSP00000242839.5:n.1286-8dup
ENST00000344297.9:c.1286-8dup	ENSP00000342559.5:n.1286-8dup
ENST00000400366.6:c.953-8dup	ENSP00000383217.3:n.953-8dup
ENST00000448424.7:c.1286-8dup	ENSP00000416738.3:n.1286-8dup
ENST00000483772.2:n.42-8dup
ENST00000673772.1:c.1286-8dup	ENSP00000501168.1:n.1286-8dup
ENST00000673789.1:n.242-8dup
ENST00000673864.1:c.480-8dup	ENSP00000501045.1:n.480-8dup
ENST00000674078.1:n.1391-12dup
ENST00000674147.1:c.842-8dup	ENSP00000500964.1:n.842-8dup
ENST00000242839.8:c.1286-8dup	ENSP00000242839.4:n.1286-8dup
ENST00000344297.8:c.1286-8dup	ENSP00000342559.5:n.1286-8dup
ENST00000400366.5:c.953-8dup	ENSP00000383217.3:n.953-8dup
ENST00000400370.8:c.1285+3178dup	ENSP00000383221.3:n.1285+3178dup
ENST00000418097.7:c.1286-8dup	ENSP00000393343.2:n.1286-8dup
ENST00000448424.6:c.1286-8dup	ENSP00000416738.2:n.1286-8dup
ENST00000482841.6:n.1407-8dup
ENST00000483772.1:n.42-8dup
ENST00000634308.1:c.1286-8dup	ENSP00000489234.1:n.1286-8dup
ENST00000634844.1:c.1286-8dup	ENSP00000489398.1:n.1286-8dup
ENST00000635406.1:n.212-24279dup
NM_000053.3:c.1286-8dup	NP_000044.2:n.1286-8dup
NM_001005918.2:c.1286-8dup	NP_001005918.1:n.1286-8dup
NM_001243182.1:c.953-8dup	NP_001230111.1:n.953-8dup
XM_005266423.2:c.1190-8dup	XP_005266480.1:n.1190-8dup
XM_005266424.3:c.1190-8dup	XP_005266481.1:n.1190-8dup
XM_005266427.2:c.1286-8dup	XP_005266484.1:n.1286-8dup
XM_005266428.1:c.1286-8dup	XP_005266485.1:n.1286-8dup
XM_005266430.3:c.1286-8dup	XP_005266487.1:n.1286-8dup
XM_005266431.2:c.1250-8dup	XP_005266488.1:n.1250-8dup
XM_005266432.2:c.1286-8dup	XP_005266489.1:n.1286-8dup
XM_006719837.2:c.1190-8dup	XP_006719900.1:n.1190-8dup
XM_011535117.1:c.1190-8dup	XP_011533419.1:n.1190-8dup
XM_011535118.1:c.1286-8dup	XP_011533420.1:n.1286-8dup
XM_011535119.1:c.1286-8dup	XP_011533421.1:n.1286-8dup
XM_011535120.1:c.1286-8dup	XP_011533422.1:n.1286-8dup
XM_011535121.1:c.1286-8dup	XP_011533423.1:n.1286-8dup
XM_011535122.1:c.-47-8dup	XP_011533424.1:n.-47-8dup
XR_941601.1:n.1505-8dup
XR_941602.1:n.1505-8dup
XR_941603.1:n.1505-8dup
XR_941604.1:n.1505-8dup
NM_001330578.1:c.1286-8dup	NP_001317507.1:n.1286-8dup
NM_001330579.1:c.1286-8dup	NP_001317508.1:n.1286-8dup
XM_005266424.4:c.1190-8dup	XP_005266481.1:n.1190-8dup
XM_005266430.4:c.1286-8dup	XP_005266487.1:n.1286-8dup
XM_005266431.4:c.1250-8dup	XP_005266488.1:n.1250-8dup
XM_006719837.3:c.1190-8dup	XP_006719900.1:n.1190-8dup
XM_011535117.3:c.1190-8dup	XP_011533419.1:n.1190-8dup
XM_017020627.1:c.1190-8dup	XP_016876116.1:n.1190-8dup
NM_000053.4:c.1286-8dup MANE Select	NP_000044.2:n.1286-8dup
NM_001005918.3:c.1286-8dup	NP_001005918.1:n.1286-8dup
NM_001330579.2:c.1286-8dup	NP_001317508.1:n.1286-8dup
NM_001243182.2:c.953-8dup	NP_001230111.1:n.953-8dup
NM_001330578.2:c.1286-8dup	NP_001317507.1:n.1286-8dup