Canonical Allele Identifier: CA388032331

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520538A>T (hg19) ; chr13:g.51946402A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946402A>T , CM000675.2:g.51946402A>T	GRCh38
NC_000013.10:g.52520538A>T , CM000675.1:g.52520538A>T	GRCh37
NC_000013.9:g.51418539A>T	NCBI36
NG_008806.1:g.70093T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*775T>A	ENSP00000489512.2:n.*775T>A
ENST00000673864.2:c.*1686T>A	ENSP00000501045.2:n.*1686T>A
ENST00000674147.2:c.2321T>A	ENSP00000500964.2:p.Ile774Asn
ENST00000242839.10:c.2942T>A MANE Select	ENSP00000242839.5:p.Ile981Asn
ENST00000344297.9:c.2321T>A	ENSP00000342559.5:p.Ile774Asn
ENST00000400366.6:c.2609T>A	ENSP00000383217.3:p.Ile870Asn
ENST00000448424.7:c.2690T>A	ENSP00000416738.3:p.Ile897Asn
ENST00000673772.1:c.2708T>A	ENSP00000501168.1:p.Ile903Asn
ENST00000673867.1:n.1089T>A
ENST00000674126.1:n.3305T>A
ENST00000674147.1:c.1877T>A	ENSP00000500964.1:p.Ile626Asn
ENST00000242839.8:c.2942T>A	ENSP00000242839.4:p.Ile981Asn
ENST00000344297.8:c.2321T>A	ENSP00000342559.5:p.Ile774Asn
ENST00000400366.5:c.2609T>A	ENSP00000383217.3:p.Ile870Asn
ENST00000400370.8:c.1652T>A	ENSP00000383221.3:p.Ile551Asn
ENST00000418097.7:c.2866-2111T>A	ENSP00000393343.2:n.2866-2111T>A
ENST00000448424.6:c.2708T>A	ENSP00000416738.2:p.Ile903Asn
ENST00000466629.1:n.162T>A
ENST00000634296.1:c.903T>A
ENST00000634308.1:c.*43T>A	ENSP00000489234.1:n.*43T>A
ENST00000634620.1:n.3686T>A
ENST00000634810.1:n.2287T>A
ENST00000634844.1:c.2798T>A	ENSP00000489398.1:p.Ile933Asn
ENST00000635406.1:n.288T>A
NM_000053.3:c.2942T>A	NP_000044.2:p.Ile981Asn
NM_001005918.2:c.2321T>A	NP_001005918.1:p.Ile774Asn
NM_001243182.1:c.2609T>A	NP_001230111.1:p.Ile870Asn
XM_005266423.2:c.2846T>A	XP_005266480.1:p.Ile949Asn
XM_005266424.3:c.2846T>A	XP_005266481.1:p.Ile949Asn
XM_005266427.2:c.2708T>A	XP_005266484.1:p.Ile903Asn
XM_005266428.1:c.2690T>A	XP_005266485.1:p.Ile897Asn
XM_005266430.3:c.2942T>A	XP_005266487.1:p.Ile981Asn
XM_005266431.2:c.2906T>A	XP_005266488.1:p.Ile969Asn
XM_005266432.2:c.2456T>A	XP_005266489.1:p.Ile819Asn
XM_006719837.2:c.2846T>A	XP_006719900.1:p.Ile949Asn
XM_006719838.1:c.758T>A	XP_006719901.1:p.Ile253Asn
XM_006719839.1:c.758T>A	XP_006719902.1:p.Ile253Asn
XM_011535117.1:c.2846T>A	XP_011533419.1:p.Ile949Asn
XM_011535118.1:c.2807T>A	XP_011533420.1:p.Ile936Asn
XM_011535119.1:c.2942T>A	XP_011533421.1:p.Ile981Asn
XM_011535120.1:c.2528T>A	XP_011533422.1:p.Ile843Asn
XM_011535121.1:c.2730+3605T>A	XP_011533423.1:n.2730+3605T>A
XM_011535122.1:c.1610T>A	XP_011533424.1:p.Ile537Asn
XR_941601.1:n.3161T>A
XR_941602.1:n.3161T>A
XR_941603.1:n.3161T>A
XR_941604.1:n.3161T>A
NM_001330578.1:c.2708T>A	NP_001317507.1:p.Ile903Asn
NM_001330579.1:c.2690T>A	NP_001317508.1:p.Ile897Asn
XM_005266424.4:c.2846T>A	XP_005266481.1:p.Ile949Asn
XM_005266430.4:c.2942T>A	XP_005266487.1:p.Ile981Asn
XM_005266431.4:c.2906T>A	XP_005266488.1:p.Ile969Asn
XM_006719837.3:c.2846T>A	XP_006719900.1:p.Ile949Asn
XM_011535117.3:c.2846T>A	XP_011533419.1:p.Ile949Asn
XM_017020627.1:c.2846T>A	XP_016876116.1:p.Ile949Asn
NM_000053.4:c.2942T>A MANE Select	NP_000044.2:p.Ile981Asn
NM_001005918.3:c.2321T>A	NP_001005918.1:p.Ile774Asn
NM_001330579.2:c.2690T>A	NP_001317508.1:p.Ile897Asn
NM_001243182.2:c.2609T>A	NP_001230111.1:p.Ile870Asn
NM_001330578.2:c.2708T>A	NP_001317507.1:p.Ile903Asn