Canonical Allele Identifier: CA388027575

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52536001G>C (hg19) ; chr13:g.51961865G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51961865G>C , CM000675.2:g.51961865G>C	GRCh38
NC_000013.10:g.52536001G>C , CM000675.1:g.52536001G>C	GRCh37
NC_000013.9:g.51434002G>C	NCBI36
NG_008806.1:g.54630C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.1918C>G	ENSP00000489512.2:p.His640Asp
ENST00000673864.2:c.*662C>G	ENSP00000501045.2:n.*662C>G
ENST00000674147.2:c.1869+3007C>G	ENSP00000500964.2:n.1869+3007C>G
ENST00000242839.10:c.1918C>G MANE Select	ENSP00000242839.5:p.His640Asp
ENST00000344297.9:c.1869+3007C>G	ENSP00000342559.5:n.1869+3007C>G
ENST00000400366.6:c.1585C>G	ENSP00000383217.3:p.His529Asp
ENST00000448424.7:c.1869+3007C>G	ENSP00000416738.3:n.1869+3007C>G
ENST00000673772.1:c.1918C>G	ENSP00000501168.1:p.His640Asp
ENST00000674147.1:c.1425+3007C>G	ENSP00000500964.1:n.1425+3007C>G
ENST00000242839.8:c.1918C>G	ENSP00000242839.4:p.His640Asp
ENST00000344297.8:c.1869+3007C>G	ENSP00000342559.5:n.1869+3007C>G
ENST00000400366.5:c.1585C>G	ENSP00000383217.3:p.His529Asp
ENST00000400370.8:c.1286-11704C>G	ENSP00000383221.3:n.1286-11704C>G
ENST00000418097.7:c.1918C>G	ENSP00000393343.2:p.His640Asp
ENST00000448424.6:c.1918C>G	ENSP00000416738.2:p.His640Asp
ENST00000482841.6:n.1665-3321C>G
ENST00000634296.1:c.54C>G
ENST00000634308.1:c.1918C>G	ENSP00000489234.1:p.His640Asp
ENST00000634620.1:n.410C>G
ENST00000634844.1:c.1918C>G	ENSP00000489398.1:p.His640Asp
ENST00000635406.1:n.212-15387C>G
NM_000053.3:c.1918C>G	NP_000044.2:p.His640Asp
NM_001005918.2:c.1869+3007C>G	NP_001005918.1:n.1869+3007C>G
NM_001243182.1:c.1585C>G	NP_001230111.1:p.His529Asp
XM_005266423.2:c.1822C>G	XP_005266480.1:p.His608Asp
XM_005266424.3:c.1822C>G	XP_005266481.1:p.His608Asp
XM_005266427.2:c.1918C>G	XP_005266484.1:p.His640Asp
XM_005266428.1:c.1869+3007C>G	XP_005266485.1:n.1869+3007C>G
XM_005266430.3:c.1918C>G	XP_005266487.1:p.His640Asp
XM_005266431.2:c.1882C>G	XP_005266488.1:p.His628Asp
XM_005266432.2:c.1869+3007C>G	XP_005266489.1:n.1869+3007C>G
XM_006719837.2:c.1822C>G	XP_006719900.1:p.His608Asp
XM_006719838.1:c.-92C>G	XP_006719901.1:n.-92C>G
XM_006719839.1:c.-92C>G	XP_006719902.1:n.-92C>G
XM_011535117.1:c.1822C>G	XP_011533419.1:p.His608Asp
XM_011535118.1:c.1918C>G	XP_011533420.1:p.His640Asp
XM_011535119.1:c.1918C>G	XP_011533421.1:p.His640Asp
XM_011535120.1:c.1708-3321C>G	XP_011533422.1:n.1708-3321C>G
XM_011535121.1:c.1918C>G	XP_011533423.1:p.His640Asp
XM_011535122.1:c.586C>G	XP_011533424.1:p.His196Asp
XR_941601.1:n.2137C>G
XR_941602.1:n.2137C>G
XR_941603.1:n.2137C>G
XR_941604.1:n.2137C>G
NM_001330578.1:c.1918C>G	NP_001317507.1:p.His640Asp
NM_001330579.1:c.1869+3007C>G	NP_001317508.1:n.1869+3007C>G
XM_005266424.4:c.1822C>G	XP_005266481.1:p.His608Asp
XM_005266430.4:c.1918C>G	XP_005266487.1:p.His640Asp
XM_005266431.4:c.1882C>G	XP_005266488.1:p.His628Asp
XM_006719837.3:c.1822C>G	XP_006719900.1:p.His608Asp
XM_011535117.3:c.1822C>G	XP_011533419.1:p.His608Asp
XM_017020627.1:c.1822C>G	XP_016876116.1:p.His608Asp
NM_000053.4:c.1918C>G MANE Select	NP_000044.2:p.His640Asp
NM_001005918.3:c.1869+3007C>G	NP_001005918.1:n.1869+3007C>G
NM_001330579.2:c.1869+3007C>G	NP_001317508.1:n.1869+3007C>G
NM_001243182.2:c.1585C>G	NP_001230111.1:p.His529Asp
NM_001330578.2:c.1918C>G	NP_001317507.1:p.His640Asp