Canonical Allele Identifier: CA388032122

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520490A>G (hg19) ; chr13:g.51946354A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*823T>C	ENSP00000489512.2:n.*823T>C
ENST00000673864.2:c.*1734T>C	ENSP00000501045.2:n.*1734T>C
ENST00000674147.2:c.2369T>C	ENSP00000500964.2:p.Val790Ala
ENST00000242839.10:c.2990T>C MANE Select	ENSP00000242839.5:p.Val997Ala
ENST00000344297.9:c.2369T>C	ENSP00000342559.5:p.Val790Ala
ENST00000400366.6:c.2657T>C	ENSP00000383217.3:p.Val886Ala
ENST00000448424.7:c.2738T>C	ENSP00000416738.3:p.Val913Ala
ENST00000673772.1:c.2756T>C	ENSP00000501168.1:p.Val919Ala
ENST00000673867.1:n.1137T>C
ENST00000674126.1:n.3353T>C
ENST00000674147.1:c.1925T>C	ENSP00000500964.1:p.Val642Ala
ENST00000242839.8:c.2990T>C	ENSP00000242839.4:p.Val997Ala
ENST00000344297.8:c.2369T>C	ENSP00000342559.5:p.Val790Ala
ENST00000400366.5:c.2657T>C	ENSP00000383217.3:p.Val886Ala
ENST00000400370.8:c.1700T>C	ENSP00000383221.3:p.Val567Ala
ENST00000418097.7:c.2866-2063T>C	ENSP00000393343.2:n.2866-2063T>C
ENST00000448424.6:c.2756T>C	ENSP00000416738.2:p.Val919Ala
ENST00000466629.1:n.210T>C
ENST00000634296.1:c.951T>C
ENST00000634308.1:c.*91T>C	ENSP00000489234.1:n.*91T>C
ENST00000634620.1:n.3734T>C
ENST00000634810.1:n.2335T>C
ENST00000634844.1:c.2846T>C	ENSP00000489398.1:p.Val949Ala
ENST00000635406.1:n.336T>C
NM_000053.3:c.2990T>C	NP_000044.2:p.Val997Ala
NM_001005918.2:c.2369T>C	NP_001005918.1:p.Val790Ala
NM_001243182.1:c.2657T>C	NP_001230111.1:p.Val886Ala
XM_005266423.2:c.2894T>C	XP_005266480.1:p.Val965Ala
XM_005266424.3:c.2894T>C	XP_005266481.1:p.Val965Ala
XM_005266427.2:c.2756T>C	XP_005266484.1:p.Val919Ala
XM_005266428.1:c.2738T>C	XP_005266485.1:p.Val913Ala
XM_005266430.3:c.2990T>C	XP_005266487.1:p.Val997Ala
XM_005266431.2:c.2954T>C	XP_005266488.1:p.Val985Ala
XM_005266432.2:c.2504T>C	XP_005266489.1:p.Val835Ala
XM_006719837.2:c.2894T>C	XP_006719900.1:p.Val965Ala
XM_006719838.1:c.806T>C	XP_006719901.1:p.Val269Ala
XM_006719839.1:c.806T>C	XP_006719902.1:p.Val269Ala
XM_011535117.1:c.2894T>C	XP_011533419.1:p.Val965Ala
XM_011535118.1:c.2855T>C	XP_011533420.1:p.Val952Ala
XM_011535119.1:c.2990T>C	XP_011533421.1:p.Val997Ala
XM_011535120.1:c.2576T>C	XP_011533422.1:p.Val859Ala
XM_011535121.1:c.2730+3653T>C	XP_011533423.1:n.2730+3653T>C
XM_011535122.1:c.1658T>C	XP_011533424.1:p.Val553Ala
XR_941601.1:n.3209T>C
XR_941602.1:n.3209T>C
XR_941603.1:n.3209T>C
XR_941604.1:n.3209T>C
NM_001330578.1:c.2756T>C	NP_001317507.1:p.Val919Ala
NM_001330579.1:c.2738T>C	NP_001317508.1:p.Val913Ala
XM_005266424.4:c.2894T>C	XP_005266481.1:p.Val965Ala
XM_005266430.4:c.2990T>C	XP_005266487.1:p.Val997Ala
XM_005266431.4:c.2954T>C	XP_005266488.1:p.Val985Ala
XM_006719837.3:c.2894T>C	XP_006719900.1:p.Val965Ala
XM_011535117.3:c.2894T>C	XP_011533419.1:p.Val965Ala
XM_017020627.1:c.2894T>C	XP_016876116.1:p.Val965Ala
NM_000053.4:c.2990T>C MANE Select	NP_000044.2:p.Val997Ala
NM_001005918.3:c.2369T>C	NP_001005918.1:p.Val790Ala
NM_001330579.2:c.2738T>C	NP_001317508.1:p.Val913Ala
NM_001243182.2:c.2657T>C	NP_001230111.1:p.Val886Ala
NM_001330578.2:c.2756T>C	NP_001317507.1:p.Val919Ala