Canonical Allele Identifier: CA388026244

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515264G>C (hg19) ; chr13:g.51941128G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941128G>C , CM000675.2:g.51941128G>C	GRCh38
NC_000013.10:g.52515264G>C , CM000675.1:g.52515264G>C	GRCh37
NC_000013.9:g.51413265G>C	NCBI36
NG_008806.1:g.75367C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1159C>G	ENSP00000489512.2:n.*1159C>G
ENST00000673864.2:c.*2253C>G	ENSP00000501045.2:n.*2253C>G
ENST00000674147.2:c.2888C>G	ENSP00000500964.2:p.Thr963Arg
ENST00000242839.10:c.3509C>G MANE Select	ENSP00000242839.5:p.Thr1170Arg
ENST00000344297.9:c.2888C>G	ENSP00000342559.5:p.Thr963Arg
ENST00000400366.6:c.3176C>G	ENSP00000383217.3:p.Thr1059Arg
ENST00000448424.7:c.3257C>G	ENSP00000416738.3:p.Thr1086Arg
ENST00000673772.1:c.3275C>G	ENSP00000501168.1:p.Thr1092Arg
ENST00000673867.1:n.3648C>G
ENST00000674126.1:n.3872C>G
ENST00000674147.1:c.2444C>G	ENSP00000500964.1:p.Thr815Arg
ENST00000242839.8:c.3509C>G	ENSP00000242839.4:p.Thr1170Arg
ENST00000344297.8:c.2888C>G	ENSP00000342559.5:p.Thr963Arg
ENST00000400366.5:c.3176C>G	ENSP00000383217.3:p.Thr1059Arg
ENST00000400370.8:c.2219C>G	ENSP00000383221.3:p.Thr740Arg
ENST00000418097.7:c.3314C>G	ENSP00000393343.2:p.Thr1105Arg
ENST00000448424.6:c.3275C>G	ENSP00000416738.2:p.Thr1092Arg
ENST00000634296.1:c.1287C>G
ENST00000634308.1:c.*610C>G	ENSP00000489234.1:n.*610C>G
ENST00000634620.1:n.4253C>G
ENST00000634810.1:n.2854C>G
ENST00000634844.1:c.3365C>G	ENSP00000489398.1:p.Thr1122Arg
NM_000053.3:c.3509C>G	NP_000044.2:p.Thr1170Arg
NM_001005918.2:c.2888C>G	NP_001005918.1:p.Thr963Arg
NM_001243182.1:c.3176C>G	NP_001230111.1:p.Thr1059Arg
XM_005266423.2:c.3413C>G	XP_005266480.1:p.Thr1138Arg
XM_005266424.3:c.3413C>G	XP_005266481.1:p.Thr1138Arg
XM_005266427.2:c.3275C>G	XP_005266484.1:p.Thr1092Arg
XM_005266428.1:c.3257C>G	XP_005266485.1:p.Thr1086Arg
XM_005266430.3:c.3509C>G	XP_005266487.1:p.Thr1170Arg
XM_005266431.2:c.3473C>G	XP_005266488.1:p.Thr1158Arg
XM_005266432.2:c.3023C>G	XP_005266489.1:p.Thr1008Arg
XM_006719837.2:c.3413C>G	XP_006719900.1:p.Thr1138Arg
XM_006719838.1:c.1325C>G	XP_006719901.1:p.Thr442Arg
XM_006719839.1:c.1142C>G	XP_006719902.1:p.Thr381Arg
XM_011535117.1:c.3413C>G	XP_011533419.1:p.Thr1138Arg
XM_011535118.1:c.3374C>G	XP_011533420.1:p.Thr1125Arg
XM_011535119.1:c.3326C>G	XP_011533421.1:p.Thr1109Arg
XM_011535120.1:c.3095C>G	XP_011533422.1:p.Thr1032Arg
XM_011535121.1:c.2996C>G	XP_011533423.1:p.Thr999Arg
XM_011535122.1:c.2177C>G	XP_011533424.1:p.Thr726Arg
XR_941601.1:n.3728C>G
XR_941602.1:n.3728C>G
XR_941603.1:n.3728C>G
XR_941604.1:n.3728C>G
NM_001330578.1:c.3275C>G	NP_001317507.1:p.Thr1092Arg
NM_001330579.1:c.3257C>G	NP_001317508.1:p.Thr1086Arg
XM_005266424.4:c.3413C>G	XP_005266481.1:p.Thr1138Arg
XM_005266430.4:c.3509C>G	XP_005266487.1:p.Thr1170Arg
XM_005266431.4:c.3473C>G	XP_005266488.1:p.Thr1158Arg
XM_006719837.3:c.3413C>G	XP_006719900.1:p.Thr1138Arg
XM_011535117.3:c.3413C>G	XP_011533419.1:p.Thr1138Arg
XM_017020627.1:c.3413C>G	XP_016876116.1:p.Thr1138Arg
NM_000053.4:c.3509C>G MANE Select	NP_000044.2:p.Thr1170Arg
NM_001005918.3:c.2888C>G	NP_001005918.1:p.Thr963Arg
NM_001330579.2:c.3257C>G	NP_001317508.1:p.Thr1086Arg
NM_001243182.2:c.3176C>G	NP_001230111.1:p.Thr1059Arg
NM_001330578.2:c.3275C>G	NP_001317507.1:p.Thr1092Arg