Canonical Allele Identifier: CA388029811

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 3071932
• ClinVar RCV Id: RCV004011962
• MyVariant Identifiers: chr13:g.52518262T>C (hg19) ; chr13:g.51944126T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944126T>C , CM000675.2:g.51944126T>C	GRCh38
NC_000013.10:g.52518262T>C , CM000675.1:g.52518262T>C	GRCh37
NC_000013.9:g.51416263T>C	NCBI36
NG_008806.1:g.72369A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1572A>G	ENSP00000489512.2:n.*894-1572A>G
ENST00000673864.2:c.*1970A>G	ENSP00000501045.2:n.*1970A>G
ENST00000674147.2:c.2605A>G	ENSP00000500964.2:p.Thr869Ala
ENST00000242839.10:c.3226A>G MANE Select	ENSP00000242839.5:p.Thr1076Ala
ENST00000344297.9:c.2605A>G	ENSP00000342559.5:p.Thr869Ala
ENST00000400366.6:c.2893A>G	ENSP00000383217.3:p.Thr965Ala
ENST00000448424.7:c.2974A>G	ENSP00000416738.3:p.Thr992Ala
ENST00000673772.1:c.2992A>G	ENSP00000501168.1:p.Thr998Ala
ENST00000673867.1:n.3365A>G
ENST00000674126.1:n.3589A>G
ENST00000674147.1:c.2161A>G	ENSP00000500964.1:p.Thr721Ala
ENST00000242839.8:c.3226A>G	ENSP00000242839.4:p.Thr1076Ala
ENST00000344297.8:c.2605A>G	ENSP00000342559.5:p.Thr869Ala
ENST00000400366.5:c.2893A>G	ENSP00000383217.3:p.Thr965Ala
ENST00000400370.8:c.1936A>G	ENSP00000383221.3:p.Thr646Ala
ENST00000418097.7:c.3031A>G	ENSP00000393343.2:p.Thr1011Ala
ENST00000448424.6:c.2992A>G	ENSP00000416738.2:p.Thr998Ala
ENST00000466629.1:n.446A>G
ENST00000634296.1:c.1022-1572A>G
ENST00000634308.1:c.*327A>G	ENSP00000489234.1:n.*327A>G
ENST00000634620.1:n.3970A>G
ENST00000634810.1:n.2571A>G
ENST00000634844.1:c.3082A>G	ENSP00000489398.1:p.Thr1028Ala
NM_000053.3:c.3226A>G	NP_000044.2:p.Thr1076Ala
NM_001005918.2:c.2605A>G	NP_001005918.1:p.Thr869Ala
NM_001243182.1:c.2893A>G	NP_001230111.1:p.Thr965Ala
XM_005266423.2:c.3130A>G	XP_005266480.1:p.Thr1044Ala
XM_005266424.3:c.3130A>G	XP_005266481.1:p.Thr1044Ala
XM_005266427.2:c.2992A>G	XP_005266484.1:p.Thr998Ala
XM_005266428.1:c.2974A>G	XP_005266485.1:p.Thr992Ala
XM_005266430.3:c.3226A>G	XP_005266487.1:p.Thr1076Ala
XM_005266431.2:c.3190A>G	XP_005266488.1:p.Thr1064Ala
XM_005266432.2:c.2740A>G	XP_005266489.1:p.Thr914Ala
XM_006719837.2:c.3130A>G	XP_006719900.1:p.Thr1044Ala
XM_006719838.1:c.1042A>G	XP_006719901.1:p.Thr348Ala
XM_006719839.1:c.877-1572A>G	XP_006719902.1:n.877-1572A>G
XM_011535117.1:c.3130A>G	XP_011533419.1:p.Thr1044Ala
XM_011535118.1:c.3091A>G	XP_011533420.1:p.Thr1031Ala
XM_011535119.1:c.3061-1572A>G	XP_011533421.1:n.3061-1572A>G
XM_011535120.1:c.2812A>G	XP_011533422.1:p.Thr938Ala
XM_011535121.1:c.2731-1572A>G	XP_011533423.1:n.2731-1572A>G
XM_011535122.1:c.1894A>G	XP_011533424.1:p.Thr632Ala
XR_941601.1:n.3445A>G
XR_941602.1:n.3445A>G
XR_941603.1:n.3445A>G
XR_941604.1:n.3445A>G
NM_001330578.1:c.2992A>G	NP_001317507.1:p.Thr998Ala
NM_001330579.1:c.2974A>G	NP_001317508.1:p.Thr992Ala
XM_005266424.4:c.3130A>G	XP_005266481.1:p.Thr1044Ala
XM_005266430.4:c.3226A>G	XP_005266487.1:p.Thr1076Ala
XM_005266431.4:c.3190A>G	XP_005266488.1:p.Thr1064Ala
XM_006719837.3:c.3130A>G	XP_006719900.1:p.Thr1044Ala
XM_011535117.3:c.3130A>G	XP_011533419.1:p.Thr1044Ala
XM_017020627.1:c.3130A>G	XP_016876116.1:p.Thr1044Ala
NM_000053.4:c.3226A>G MANE Select	NP_000044.2:p.Thr1076Ala
NM_001005918.3:c.2605A>G	NP_001005918.1:p.Thr869Ala
NM_001330579.2:c.2974A>G	NP_001317508.1:p.Thr992Ala
NM_001243182.2:c.2893A>G	NP_001230111.1:p.Thr965Ala
NM_001330578.2:c.2992A>G	NP_001317507.1:p.Thr998Ala