Canonical Allele Identifier: CA388024348

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513286C>G (hg19) ; chr13:g.51939150C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939150C>G , CM000675.2:g.51939150C>G	GRCh38
NC_000013.10:g.52513286C>G , CM000675.1:g.52513286C>G	GRCh37
NC_000013.9:g.51411287C>G	NCBI36
NG_008806.1:g.77345G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1250G>C	ENSP00000489512.2:n.*1250G>C
ENST00000673864.2:c.*2344G>C	ENSP00000501045.2:n.*2344G>C
ENST00000674147.2:c.2979G>C	ENSP00000500964.2:p.Gln993His
ENST00000242839.10:c.3600G>C MANE Select	ENSP00000242839.5:p.Gln1200His
ENST00000344297.9:c.2979G>C	ENSP00000342559.5:p.Gln993His
ENST00000400366.6:c.3267G>C	ENSP00000383217.3:p.Gln1089His
ENST00000448424.7:c.3348G>C	ENSP00000416738.3:p.Gln1116His
ENST00000673696.1:n.841G>C
ENST00000673772.1:c.3366G>C	ENSP00000501168.1:p.Gln1122His
ENST00000673867.1:n.3739G>C
ENST00000673923.1:n.466G>C
ENST00000674147.1:c.2535G>C	ENSP00000500964.1:p.Gln845His
ENST00000242839.8:c.3600G>C	ENSP00000242839.4:p.Gln1200His
ENST00000344297.8:c.2979G>C	ENSP00000342559.5:p.Gln993His
ENST00000400366.5:c.3267G>C	ENSP00000383217.3:p.Gln1089His
ENST00000400370.8:c.2310G>C	ENSP00000383221.3:p.Gln770His
ENST00000418097.7:c.3405G>C	ENSP00000393343.2:p.Gln1135His
ENST00000448424.6:c.3366G>C	ENSP00000416738.2:p.Gln1122His
ENST00000634296.1:c.1378G>C
ENST00000634308.1:c.*701G>C	ENSP00000489234.1:n.*701G>C
ENST00000634620.1:n.4344G>C
ENST00000634810.1:n.2945G>C
ENST00000634844.1:c.3456G>C	ENSP00000489398.1:p.Gln1152His
NM_000053.3:c.3600G>C	NP_000044.2:p.Gln1200His
NM_001005918.2:c.2979G>C	NP_001005918.1:p.Gln993His
NM_001243182.1:c.3267G>C	NP_001230111.1:p.Gln1089His
XM_005266423.2:c.3504G>C	XP_005266480.1:p.Gln1168His
XM_005266424.3:c.3504G>C	XP_005266481.1:p.Gln1168His
XM_005266427.2:c.3366G>C	XP_005266484.1:p.Gln1122His
XM_005266428.1:c.3348G>C	XP_005266485.1:p.Gln1116His
XM_005266430.3:c.3600G>C	XP_005266487.1:p.Gln1200His
XM_005266431.2:c.3564G>C	XP_005266488.1:p.Gln1188His
XM_005266432.2:c.3114G>C	XP_005266489.1:p.Gln1038His
XM_006719837.2:c.3504G>C	XP_006719900.1:p.Gln1168His
XM_006719838.1:c.1416G>C	XP_006719901.1:p.Gln472His
XM_006719839.1:c.1233G>C	XP_006719902.1:p.Gln411His
XM_011535117.1:c.3504G>C	XP_011533419.1:p.Gln1168His
XM_011535118.1:c.3465G>C	XP_011533420.1:p.Gln1155His
XM_011535119.1:c.3417G>C	XP_011533421.1:p.Gln1139His
XM_011535120.1:c.3186G>C	XP_011533422.1:p.Gln1062His
XM_011535121.1:c.3087G>C	XP_011533423.1:p.Gln1029His
XM_011535122.1:c.2268G>C	XP_011533424.1:p.Gln756His
XR_941601.1:n.3819G>C
XR_941602.1:n.3819G>C
XR_941603.1:n.3819G>C
XR_941604.1:n.3819G>C
NM_001330578.1:c.3366G>C	NP_001317507.1:p.Gln1122His
NM_001330579.1:c.3348G>C	NP_001317508.1:p.Gln1116His
XM_005266424.4:c.3504G>C	XP_005266481.1:p.Gln1168His
XM_005266430.4:c.3600G>C	XP_005266487.1:p.Gln1200His
XM_005266431.4:c.3564G>C	XP_005266488.1:p.Gln1188His
XM_006719837.3:c.3504G>C	XP_006719900.1:p.Gln1168His
XM_011535117.3:c.3504G>C	XP_011533419.1:p.Gln1168His
XM_017020627.1:c.3504G>C	XP_016876116.1:p.Gln1168His
NM_000053.4:c.3600G>C MANE Select	NP_000044.2:p.Gln1200His
NM_001005918.3:c.2979G>C	NP_001005918.1:p.Gln993His
NM_001330579.2:c.3348G>C	NP_001317508.1:p.Gln1116His
NM_001243182.2:c.3267G>C	NP_001230111.1:p.Gln1089His
NM_001330578.2:c.3366G>C	NP_001317507.1:p.Gln1122His