Canonical Allele Identifier: CA388020866

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52511439T>C (hg19) ; chr13:g.51937303T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51937303T>C , CM000675.2:g.51937303T>C	GRCh38
NC_000013.10:g.52511439T>C , CM000675.1:g.52511439T>C	GRCh37
NC_000013.9:g.51409440T>C	NCBI36
NG_008806.1:g.79192A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1644A>G	ENSP00000489512.2:n.*1644A>G
ENST00000673864.2:c.*2738A>G	ENSP00000501045.2:n.*2738A>G
ENST00000674147.2:c.3373A>G	ENSP00000500964.2:p.Asn1125Asp
ENST00000242839.10:c.3994A>G MANE Select	ENSP00000242839.5:p.Asn1332Asp
ENST00000344297.9:c.3373A>G	ENSP00000342559.5:p.Asn1125Asp
ENST00000400366.6:c.3661A>G	ENSP00000383217.3:p.Asn1221Asp
ENST00000448424.7:c.3742A>G	ENSP00000416738.3:p.Asn1248Asp
ENST00000673696.1:n.1317A>G
ENST00000673772.1:c.3760A>G	ENSP00000501168.1:p.Asn1254Asp
ENST00000673867.1:n.4133A>G
ENST00000673923.1:n.860A>G
ENST00000674147.1:c.2929A>G	ENSP00000500964.1:p.Asn977Asp
ENST00000242839.8:c.3994A>G	ENSP00000242839.4:p.Asn1332Asp
ENST00000344297.8:c.3373A>G	ENSP00000342559.5:p.Asn1125Asp
ENST00000400366.5:c.3661A>G	ENSP00000383217.3:p.Asn1221Asp
ENST00000400370.8:c.2704A>G	ENSP00000383221.3:p.Asn902Asp
ENST00000418097.7:c.3799A>G	ENSP00000393343.2:p.Asn1267Asp
ENST00000448424.6:c.3760A>G	ENSP00000416738.2:p.Asn1254Asp
ENST00000634296.1:c.1772A>G
ENST00000634308.1:c.*1095A>G	ENSP00000489234.1:n.*1095A>G
ENST00000634620.1:n.4738A>G
ENST00000634810.1:n.3339A>G
ENST00000634844.1:c.3850A>G	ENSP00000489398.1:p.Asn1284Asp
NM_000053.3:c.3994A>G	NP_000044.2:p.Asn1332Asp
NM_001005918.2:c.3373A>G	NP_001005918.1:p.Asn1125Asp
NM_001243182.1:c.3661A>G	NP_001230111.1:p.Asn1221Asp
XM_005266423.2:c.3898A>G	XP_005266480.1:p.Asn1300Asp
XM_005266424.3:c.3898A>G	XP_005266481.1:p.Asn1300Asp
XM_005266427.2:c.3760A>G	XP_005266484.1:p.Asn1254Asp
XM_005266428.1:c.3742A>G	XP_005266485.1:p.Asn1248Asp
XM_005266430.3:c.3994A>G	XP_005266487.1:p.Asn1332Asp
XM_005266431.2:c.3958A>G	XP_005266488.1:p.Asn1320Asp
XM_005266432.2:c.3508A>G	XP_005266489.1:p.Asn1170Asp
XM_006719837.2:c.3898A>G	XP_006719900.1:p.Asn1300Asp
XM_006719838.1:c.1810A>G	XP_006719901.1:p.Asn604Asp
XM_006719839.1:c.1627A>G	XP_006719902.1:p.Asn543Asp
XM_011535117.1:c.3898A>G	XP_011533419.1:p.Asn1300Asp
XM_011535118.1:c.3859A>G	XP_011533420.1:p.Asn1287Asp
XM_011535119.1:c.3811A>G	XP_011533421.1:p.Asn1271Asp
XM_011535120.1:c.3580A>G	XP_011533422.1:p.Asn1194Asp
XM_011535121.1:c.3481A>G	XP_011533423.1:p.Asn1161Asp
XM_011535122.1:c.2662A>G	XP_011533424.1:p.Asn888Asp
XR_941601.1:n.4213A>G
XR_941602.1:n.4213A>G
XR_941603.1:n.4213A>G
XR_941604.1:n.4213A>G
NM_001330578.1:c.3760A>G	NP_001317507.1:p.Asn1254Asp
NM_001330579.1:c.3742A>G	NP_001317508.1:p.Asn1248Asp
XM_005266424.4:c.3898A>G	XP_005266481.1:p.Asn1300Asp
XM_005266430.4:c.3994A>G	XP_005266487.1:p.Asn1332Asp
XM_005266431.4:c.3958A>G	XP_005266488.1:p.Asn1320Asp
XM_006719837.3:c.3898A>G	XP_006719900.1:p.Asn1300Asp
XM_011535117.3:c.3898A>G	XP_011533419.1:p.Asn1300Asp
XM_017020627.1:c.3898A>G	XP_016876116.1:p.Asn1300Asp
NM_000053.4:c.3994A>G MANE Select	NP_000044.2:p.Asn1332Asp
NM_001005918.3:c.3373A>G	NP_001005918.1:p.Asn1125Asp
NM_001330579.2:c.3742A>G	NP_001317508.1:p.Asn1248Asp
NM_001243182.2:c.3661A>G	NP_001230111.1:p.Asn1221Asp
NM_001330578.2:c.3760A>G	NP_001317507.1:p.Asn1254Asp