Canonical Allele Identifier: CA483893817

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513301T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939165T>C , CM000675.2:g.51939165T>C	GRCh38
NC_000013.10:g.52513301T>C , CM000675.1:g.52513301T>C	GRCh37
NC_000013.9:g.51411302T>C	NCBI36
NG_008806.1:g.77330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1235A>G	ENSP00000489512.2:n.*1235A>G
ENST00000673864.2:c.*2329A>G	ENSP00000501045.2:n.*2329A>G
ENST00000674147.2:c.2964A>G	ENSP00000500964.2:p.Ala988=
ENST00000242839.10:c.3585A>G MANE Select	ENSP00000242839.5:p.Ala1195=
ENST00000344297.9:c.2964A>G	ENSP00000342559.5:p.Ala988=
ENST00000400366.6:c.3252A>G	ENSP00000383217.3:p.Ala1084=
ENST00000448424.7:c.3333A>G	ENSP00000416738.3:p.Ala1111=
ENST00000673696.1:n.826A>G
ENST00000673772.1:c.3351A>G	ENSP00000501168.1:p.Ala1117=
ENST00000673867.1:n.3724A>G
ENST00000673923.1:n.451A>G
ENST00000674147.1:c.2520A>G	ENSP00000500964.1:p.Ala840=
ENST00000242839.8:c.3585A>G	ENSP00000242839.4:p.Ala1195=
ENST00000344297.8:c.2964A>G	ENSP00000342559.5:p.Ala988=
ENST00000400366.5:c.3252A>G	ENSP00000383217.3:p.Ala1084=
ENST00000400370.8:c.2295A>G	ENSP00000383221.3:p.Ala765=
ENST00000418097.7:c.3390A>G	ENSP00000393343.2:p.Ala1130=
ENST00000448424.6:c.3351A>G	ENSP00000416738.2:p.Ala1117=
ENST00000634296.1:c.1363A>G
ENST00000634308.1:c.*686A>G	ENSP00000489234.1:n.*686A>G
ENST00000634620.1:n.4329A>G
ENST00000634810.1:n.2930A>G
ENST00000634844.1:c.3441A>G	ENSP00000489398.1:p.Ala1147=
NM_000053.3:c.3585A>G	NP_000044.2:p.Ala1195=
NM_001005918.2:c.2964A>G	NP_001005918.1:p.Ala988=
NM_001243182.1:c.3252A>G	NP_001230111.1:p.Ala1084=
XM_005266423.2:c.3489A>G	XP_005266480.1:p.Ala1163=
XM_005266424.3:c.3489A>G	XP_005266481.1:p.Ala1163=
XM_005266427.2:c.3351A>G	XP_005266484.1:p.Ala1117=
XM_005266428.1:c.3333A>G	XP_005266485.1:p.Ala1111=
XM_005266430.3:c.3585A>G	XP_005266487.1:p.Ala1195=
XM_005266431.2:c.3549A>G	XP_005266488.1:p.Ala1183=
XM_005266432.2:c.3099A>G	XP_005266489.1:p.Ala1033=
XM_006719837.2:c.3489A>G	XP_006719900.1:p.Ala1163=
XM_006719838.1:c.1401A>G	XP_006719901.1:p.Ala467=
XM_006719839.1:c.1218A>G	XP_006719902.1:p.Ala406=
XM_011535117.1:c.3489A>G	XP_011533419.1:p.Ala1163=
XM_011535118.1:c.3450A>G	XP_011533420.1:p.Ala1150=
XM_011535119.1:c.3402A>G	XP_011533421.1:p.Ala1134=
XM_011535120.1:c.3171A>G	XP_011533422.1:p.Ala1057=
XM_011535121.1:c.3072A>G	XP_011533423.1:p.Ala1024=
XM_011535122.1:c.2253A>G	XP_011533424.1:p.Ala751=
XR_941601.1:n.3804A>G
XR_941602.1:n.3804A>G
XR_941603.1:n.3804A>G
XR_941604.1:n.3804A>G
NM_001330578.1:c.3351A>G	NP_001317507.1:p.Ala1117=
NM_001330579.1:c.3333A>G	NP_001317508.1:p.Ala1111=
XM_005266424.4:c.3489A>G	XP_005266481.1:p.Ala1163=
XM_005266430.4:c.3585A>G	XP_005266487.1:p.Ala1195=
XM_005266431.4:c.3549A>G	XP_005266488.1:p.Ala1183=
XM_006719837.3:c.3489A>G	XP_006719900.1:p.Ala1163=
XM_011535117.3:c.3489A>G	XP_011533419.1:p.Ala1163=
XM_017020627.1:c.3489A>G	XP_016876116.1:p.Ala1163=
NM_000053.4:c.3585A>G MANE Select	NP_000044.2:p.Ala1195=
NM_001005918.3:c.2964A>G	NP_001005918.1:p.Ala988=
NM_001330579.2:c.3333A>G	NP_001317508.1:p.Ala1111=
NM_001243182.2:c.3252A>G	NP_001230111.1:p.Ala1084=
NM_001330578.2:c.3351A>G	NP_001317507.1:p.Ala1117=