Canonical Allele Identifier: CA388029808

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518261G>T (hg19) ; chr13:g.51944125G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944125G>T , CM000675.2:g.51944125G>T	GRCh38
NC_000013.10:g.52518261G>T , CM000675.1:g.52518261G>T	GRCh37
NC_000013.9:g.51416262G>T	NCBI36
NG_008806.1:g.72370C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1571C>A	ENSP00000489512.2:n.*894-1571C>A
ENST00000673864.2:c.*1971C>A	ENSP00000501045.2:n.*1971C>A
ENST00000674147.2:c.2606C>A	ENSP00000500964.2:p.Thr869Asn
ENST00000242839.10:c.3227C>A MANE Select	ENSP00000242839.5:p.Thr1076Asn
ENST00000344297.9:c.2606C>A	ENSP00000342559.5:p.Thr869Asn
ENST00000400366.6:c.2894C>A	ENSP00000383217.3:p.Thr965Asn
ENST00000448424.7:c.2975C>A	ENSP00000416738.3:p.Thr992Asn
ENST00000673772.1:c.2993C>A	ENSP00000501168.1:p.Thr998Asn
ENST00000673867.1:n.3366C>A
ENST00000674126.1:n.3590C>A
ENST00000674147.1:c.2162C>A	ENSP00000500964.1:p.Thr721Asn
ENST00000242839.8:c.3227C>A	ENSP00000242839.4:p.Thr1076Asn
ENST00000344297.8:c.2606C>A	ENSP00000342559.5:p.Thr869Asn
ENST00000400366.5:c.2894C>A	ENSP00000383217.3:p.Thr965Asn
ENST00000400370.8:c.1937C>A	ENSP00000383221.3:p.Thr646Asn
ENST00000418097.7:c.3032C>A	ENSP00000393343.2:p.Thr1011Asn
ENST00000448424.6:c.2993C>A	ENSP00000416738.2:p.Thr998Asn
ENST00000466629.1:n.447C>A
ENST00000634296.1:c.1022-1571C>A
ENST00000634308.1:c.*328C>A	ENSP00000489234.1:n.*328C>A
ENST00000634620.1:n.3971C>A
ENST00000634810.1:n.2572C>A
ENST00000634844.1:c.3083C>A	ENSP00000489398.1:p.Thr1028Asn
NM_000053.3:c.3227C>A	NP_000044.2:p.Thr1076Asn
NM_001005918.2:c.2606C>A	NP_001005918.1:p.Thr869Asn
NM_001243182.1:c.2894C>A	NP_001230111.1:p.Thr965Asn
XM_005266423.2:c.3131C>A	XP_005266480.1:p.Thr1044Asn
XM_005266424.3:c.3131C>A	XP_005266481.1:p.Thr1044Asn
XM_005266427.2:c.2993C>A	XP_005266484.1:p.Thr998Asn
XM_005266428.1:c.2975C>A	XP_005266485.1:p.Thr992Asn
XM_005266430.3:c.3227C>A	XP_005266487.1:p.Thr1076Asn
XM_005266431.2:c.3191C>A	XP_005266488.1:p.Thr1064Asn
XM_005266432.2:c.2741C>A	XP_005266489.1:p.Thr914Asn
XM_006719837.2:c.3131C>A	XP_006719900.1:p.Thr1044Asn
XM_006719838.1:c.1043C>A	XP_006719901.1:p.Thr348Asn
XM_006719839.1:c.877-1571C>A	XP_006719902.1:n.877-1571C>A
XM_011535117.1:c.3131C>A	XP_011533419.1:p.Thr1044Asn
XM_011535118.1:c.3092C>A	XP_011533420.1:p.Thr1031Asn
XM_011535119.1:c.3061-1571C>A	XP_011533421.1:n.3061-1571C>A
XM_011535120.1:c.2813C>A	XP_011533422.1:p.Thr938Asn
XM_011535121.1:c.2731-1571C>A	XP_011533423.1:n.2731-1571C>A
XM_011535122.1:c.1895C>A	XP_011533424.1:p.Thr632Asn
XR_941601.1:n.3446C>A
XR_941602.1:n.3446C>A
XR_941603.1:n.3446C>A
XR_941604.1:n.3446C>A
NM_001330578.1:c.2993C>A	NP_001317507.1:p.Thr998Asn
NM_001330579.1:c.2975C>A	NP_001317508.1:p.Thr992Asn
XM_005266424.4:c.3131C>A	XP_005266481.1:p.Thr1044Asn
XM_005266430.4:c.3227C>A	XP_005266487.1:p.Thr1076Asn
XM_005266431.4:c.3191C>A	XP_005266488.1:p.Thr1064Asn
XM_006719837.3:c.3131C>A	XP_006719900.1:p.Thr1044Asn
XM_011535117.3:c.3131C>A	XP_011533419.1:p.Thr1044Asn
XM_017020627.1:c.3131C>A	XP_016876116.1:p.Thr1044Asn
NM_000053.4:c.3227C>A MANE Select	NP_000044.2:p.Thr1076Asn
NM_001005918.3:c.2606C>A	NP_001005918.1:p.Thr869Asn
NM_001330579.2:c.2975C>A	NP_001317508.1:p.Thr992Asn
NM_001243182.2:c.2894C>A	NP_001230111.1:p.Thr965Asn
NM_001330578.2:c.2993C>A	NP_001317507.1:p.Thr998Asn