Canonical Allele Identifier: CA388026654

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515325T>A (hg19) ; chr13:g.51941189T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941189T>A , CM000675.2:g.51941189T>A	GRCh38
NC_000013.10:g.52515325T>A , CM000675.1:g.52515325T>A	GRCh37
NC_000013.9:g.51413326T>A	NCBI36
NG_008806.1:g.75306A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1098A>T	ENSP00000489512.2:n.*1098A>T
ENST00000673864.2:c.*2192A>T	ENSP00000501045.2:n.*2192A>T
ENST00000674147.2:c.2827A>T	ENSP00000500964.2:p.Asn943Tyr
ENST00000242839.10:c.3448A>T MANE Select	ENSP00000242839.5:p.Asn1150Tyr
ENST00000344297.9:c.2827A>T	ENSP00000342559.5:p.Asn943Tyr
ENST00000400366.6:c.3115A>T	ENSP00000383217.3:p.Asn1039Tyr
ENST00000448424.7:c.3196A>T	ENSP00000416738.3:p.Asn1066Tyr
ENST00000673772.1:c.3214A>T	ENSP00000501168.1:p.Asn1072Tyr
ENST00000673867.1:n.3587A>T
ENST00000674126.1:n.3811A>T
ENST00000674147.1:c.2383A>T	ENSP00000500964.1:p.Asn795Tyr
ENST00000242839.8:c.3448A>T	ENSP00000242839.4:p.Asn1150Tyr
ENST00000344297.8:c.2827A>T	ENSP00000342559.5:p.Asn943Tyr
ENST00000400366.5:c.3115A>T	ENSP00000383217.3:p.Asn1039Tyr
ENST00000400370.8:c.2158A>T	ENSP00000383221.3:p.Asn720Tyr
ENST00000418097.7:c.3253A>T	ENSP00000393343.2:p.Asn1085Tyr
ENST00000448424.6:c.3214A>T	ENSP00000416738.2:p.Asn1072Tyr
ENST00000634296.1:c.1226A>T
ENST00000634308.1:c.*549A>T	ENSP00000489234.1:n.*549A>T
ENST00000634620.1:n.4192A>T
ENST00000634810.1:n.2793A>T
ENST00000634844.1:c.3304A>T	ENSP00000489398.1:p.Asn1102Tyr
NM_000053.3:c.3448A>T	NP_000044.2:p.Asn1150Tyr
NM_001005918.2:c.2827A>T	NP_001005918.1:p.Asn943Tyr
NM_001243182.1:c.3115A>T	NP_001230111.1:p.Asn1039Tyr
XM_005266423.2:c.3352A>T	XP_005266480.1:p.Asn1118Tyr
XM_005266424.3:c.3352A>T	XP_005266481.1:p.Asn1118Tyr
XM_005266427.2:c.3214A>T	XP_005266484.1:p.Asn1072Tyr
XM_005266428.1:c.3196A>T	XP_005266485.1:p.Asn1066Tyr
XM_005266430.3:c.3448A>T	XP_005266487.1:p.Asn1150Tyr
XM_005266431.2:c.3412A>T	XP_005266488.1:p.Asn1138Tyr
XM_005266432.2:c.2962A>T	XP_005266489.1:p.Asn988Tyr
XM_006719837.2:c.3352A>T	XP_006719900.1:p.Asn1118Tyr
XM_006719838.1:c.1264A>T	XP_006719901.1:p.Asn422Tyr
XM_006719839.1:c.1081A>T	XP_006719902.1:p.Asn361Tyr
XM_011535117.1:c.3352A>T	XP_011533419.1:p.Asn1118Tyr
XM_011535118.1:c.3313A>T	XP_011533420.1:p.Asn1105Tyr
XM_011535119.1:c.3265A>T	XP_011533421.1:p.Asn1089Tyr
XM_011535120.1:c.3034A>T	XP_011533422.1:p.Asn1012Tyr
XM_011535121.1:c.2935A>T	XP_011533423.1:p.Asn979Tyr
XM_011535122.1:c.2116A>T	XP_011533424.1:p.Asn706Tyr
XR_941601.1:n.3667A>T
XR_941602.1:n.3667A>T
XR_941603.1:n.3667A>T
XR_941604.1:n.3667A>T
NM_001330578.1:c.3214A>T	NP_001317507.1:p.Asn1072Tyr
NM_001330579.1:c.3196A>T	NP_001317508.1:p.Asn1066Tyr
XM_005266424.4:c.3352A>T	XP_005266481.1:p.Asn1118Tyr
XM_005266430.4:c.3448A>T	XP_005266487.1:p.Asn1150Tyr
XM_005266431.4:c.3412A>T	XP_005266488.1:p.Asn1138Tyr
XM_006719837.3:c.3352A>T	XP_006719900.1:p.Asn1118Tyr
XM_011535117.3:c.3352A>T	XP_011533419.1:p.Asn1118Tyr
XM_017020627.1:c.3352A>T	XP_016876116.1:p.Asn1118Tyr
NM_000053.4:c.3448A>T MANE Select	NP_000044.2:p.Asn1150Tyr
NM_001005918.3:c.2827A>T	NP_001005918.1:p.Asn943Tyr
NM_001330579.2:c.3196A>T	NP_001317508.1:p.Asn1066Tyr
NM_001243182.2:c.3115A>T	NP_001230111.1:p.Asn1039Tyr
NM_001330578.2:c.3214A>T	NP_001317507.1:p.Asn1072Tyr