Canonical Allele Identifier: CA388032119

Gene: ATP7B

Linked Data

• dbSNP Id: rs1593681073
• MyVariant Identifiers: chr13:g.52520490A>C (hg19) ; chr13:g.51946354A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946354A>C , CM000675.2:g.51946354A>C	GRCh38
NC_000013.10:g.52520490A>C , CM000675.1:g.52520490A>C	GRCh37
NC_000013.9:g.51418491A>C	NCBI36
NG_008806.1:g.70141T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*823T>G	ENSP00000489512.2:n.*823T>G
ENST00000673864.2:c.*1734T>G	ENSP00000501045.2:n.*1734T>G
ENST00000674147.2:c.2369T>G	ENSP00000500964.2:p.Val790Gly
ENST00000242839.10:c.2990T>G MANE Select	ENSP00000242839.5:p.Val997Gly
ENST00000344297.9:c.2369T>G	ENSP00000342559.5:p.Val790Gly
ENST00000400366.6:c.2657T>G	ENSP00000383217.3:p.Val886Gly
ENST00000448424.7:c.2738T>G	ENSP00000416738.3:p.Val913Gly
ENST00000673772.1:c.2756T>G	ENSP00000501168.1:p.Val919Gly
ENST00000673867.1:n.1137T>G
ENST00000674126.1:n.3353T>G
ENST00000674147.1:c.1925T>G	ENSP00000500964.1:p.Val642Gly
ENST00000242839.8:c.2990T>G	ENSP00000242839.4:p.Val997Gly
ENST00000344297.8:c.2369T>G	ENSP00000342559.5:p.Val790Gly
ENST00000400366.5:c.2657T>G	ENSP00000383217.3:p.Val886Gly
ENST00000400370.8:c.1700T>G	ENSP00000383221.3:p.Val567Gly
ENST00000418097.7:c.2866-2063T>G	ENSP00000393343.2:n.2866-2063T>G
ENST00000448424.6:c.2756T>G	ENSP00000416738.2:p.Val919Gly
ENST00000466629.1:n.210T>G
ENST00000634296.1:c.951T>G
ENST00000634308.1:c.*91T>G	ENSP00000489234.1:n.*91T>G
ENST00000634620.1:n.3734T>G
ENST00000634810.1:n.2335T>G
ENST00000634844.1:c.2846T>G	ENSP00000489398.1:p.Val949Gly
ENST00000635406.1:n.336T>G
NM_000053.3:c.2990T>G	NP_000044.2:p.Val997Gly
NM_001005918.2:c.2369T>G	NP_001005918.1:p.Val790Gly
NM_001243182.1:c.2657T>G	NP_001230111.1:p.Val886Gly
XM_005266423.2:c.2894T>G	XP_005266480.1:p.Val965Gly
XM_005266424.3:c.2894T>G	XP_005266481.1:p.Val965Gly
XM_005266427.2:c.2756T>G	XP_005266484.1:p.Val919Gly
XM_005266428.1:c.2738T>G	XP_005266485.1:p.Val913Gly
XM_005266430.3:c.2990T>G	XP_005266487.1:p.Val997Gly
XM_005266431.2:c.2954T>G	XP_005266488.1:p.Val985Gly
XM_005266432.2:c.2504T>G	XP_005266489.1:p.Val835Gly
XM_006719837.2:c.2894T>G	XP_006719900.1:p.Val965Gly
XM_006719838.1:c.806T>G	XP_006719901.1:p.Val269Gly
XM_006719839.1:c.806T>G	XP_006719902.1:p.Val269Gly
XM_011535117.1:c.2894T>G	XP_011533419.1:p.Val965Gly
XM_011535118.1:c.2855T>G	XP_011533420.1:p.Val952Gly
XM_011535119.1:c.2990T>G	XP_011533421.1:p.Val997Gly
XM_011535120.1:c.2576T>G	XP_011533422.1:p.Val859Gly
XM_011535121.1:c.2730+3653T>G	XP_011533423.1:n.2730+3653T>G
XM_011535122.1:c.1658T>G	XP_011533424.1:p.Val553Gly
XR_941601.1:n.3209T>G
XR_941602.1:n.3209T>G
XR_941603.1:n.3209T>G
XR_941604.1:n.3209T>G
NM_001330578.1:c.2756T>G	NP_001317507.1:p.Val919Gly
NM_001330579.1:c.2738T>G	NP_001317508.1:p.Val913Gly
XM_005266424.4:c.2894T>G	XP_005266481.1:p.Val965Gly
XM_005266430.4:c.2990T>G	XP_005266487.1:p.Val997Gly
XM_005266431.4:c.2954T>G	XP_005266488.1:p.Val985Gly
XM_006719837.3:c.2894T>G	XP_006719900.1:p.Val965Gly
XM_011535117.3:c.2894T>G	XP_011533419.1:p.Val965Gly
XM_017020627.1:c.2894T>G	XP_016876116.1:p.Val965Gly
NM_000053.4:c.2990T>G MANE Select	NP_000044.2:p.Val997Gly
NM_001005918.3:c.2369T>G	NP_001005918.1:p.Val790Gly
NM_001330579.2:c.2738T>G	NP_001317508.1:p.Val913Gly
NM_001243182.2:c.2657T>G	NP_001230111.1:p.Val886Gly
NM_001330578.2:c.2756T>G	NP_001317507.1:p.Val919Gly