Canonical Allele Identifier: CA388023976

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513243C>A (hg19) ; chr13:g.51939107C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939107C>A , CM000675.2:g.51939107C>A	GRCh38
NC_000013.10:g.52513243C>A , CM000675.1:g.52513243C>A	GRCh37
NC_000013.9:g.51411244C>A	NCBI36
NG_008806.1:g.77388G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1293G>T	ENSP00000489512.2:n.*1293G>T
ENST00000673864.2:c.*2387G>T	ENSP00000501045.2:n.*2387G>T
ENST00000674147.2:c.3022G>T	ENSP00000500964.2:p.Asp1008Tyr
ENST00000242839.10:c.3643G>T MANE Select	ENSP00000242839.5:p.Asp1215Tyr
ENST00000344297.9:c.3022G>T	ENSP00000342559.5:p.Asp1008Tyr
ENST00000400366.6:c.3310G>T	ENSP00000383217.3:p.Asp1104Tyr
ENST00000448424.7:c.3391G>T	ENSP00000416738.3:p.Asp1131Tyr
ENST00000673696.1:n.884G>T
ENST00000673772.1:c.3409G>T	ENSP00000501168.1:p.Asp1137Tyr
ENST00000673867.1:n.3782G>T
ENST00000673923.1:n.509G>T
ENST00000674147.1:c.2578G>T	ENSP00000500964.1:p.Asp860Tyr
ENST00000242839.8:c.3643G>T	ENSP00000242839.4:p.Asp1215Tyr
ENST00000344297.8:c.3022G>T	ENSP00000342559.5:p.Asp1008Tyr
ENST00000400366.5:c.3310G>T	ENSP00000383217.3:p.Asp1104Tyr
ENST00000400370.8:c.2353G>T	ENSP00000383221.3:p.Asp785Tyr
ENST00000418097.7:c.3448G>T	ENSP00000393343.2:p.Asp1150Tyr
ENST00000448424.6:c.3409G>T	ENSP00000416738.2:p.Asp1137Tyr
ENST00000634296.1:c.1421G>T
ENST00000634308.1:c.*744G>T	ENSP00000489234.1:n.*744G>T
ENST00000634620.1:n.4387G>T
ENST00000634810.1:n.2988G>T
ENST00000634844.1:c.3499G>T	ENSP00000489398.1:p.Asp1167Tyr
NM_000053.3:c.3643G>T	NP_000044.2:p.Asp1215Tyr
NM_001005918.2:c.3022G>T	NP_001005918.1:p.Asp1008Tyr
NM_001243182.1:c.3310G>T	NP_001230111.1:p.Asp1104Tyr
XM_005266423.2:c.3547G>T	XP_005266480.1:p.Asp1183Tyr
XM_005266424.3:c.3547G>T	XP_005266481.1:p.Asp1183Tyr
XM_005266427.2:c.3409G>T	XP_005266484.1:p.Asp1137Tyr
XM_005266428.1:c.3391G>T	XP_005266485.1:p.Asp1131Tyr
XM_005266430.3:c.3643G>T	XP_005266487.1:p.Asp1215Tyr
XM_005266431.2:c.3607G>T	XP_005266488.1:p.Asp1203Tyr
XM_005266432.2:c.3157G>T	XP_005266489.1:p.Asp1053Tyr
XM_006719837.2:c.3547G>T	XP_006719900.1:p.Asp1183Tyr
XM_006719838.1:c.1459G>T	XP_006719901.1:p.Asp487Tyr
XM_006719839.1:c.1276G>T	XP_006719902.1:p.Asp426Tyr
XM_011535117.1:c.3547G>T	XP_011533419.1:p.Asp1183Tyr
XM_011535118.1:c.3508G>T	XP_011533420.1:p.Asp1170Tyr
XM_011535119.1:c.3460G>T	XP_011533421.1:p.Asp1154Tyr
XM_011535120.1:c.3229G>T	XP_011533422.1:p.Asp1077Tyr
XM_011535121.1:c.3130G>T	XP_011533423.1:p.Asp1044Tyr
XM_011535122.1:c.2311G>T	XP_011533424.1:p.Asp771Tyr
XR_941601.1:n.3862G>T
XR_941602.1:n.3862G>T
XR_941603.1:n.3862G>T
XR_941604.1:n.3862G>T
NM_001330578.1:c.3409G>T	NP_001317507.1:p.Asp1137Tyr
NM_001330579.1:c.3391G>T	NP_001317508.1:p.Asp1131Tyr
XM_005266424.4:c.3547G>T	XP_005266481.1:p.Asp1183Tyr
XM_005266430.4:c.3643G>T	XP_005266487.1:p.Asp1215Tyr
XM_005266431.4:c.3607G>T	XP_005266488.1:p.Asp1203Tyr
XM_006719837.3:c.3547G>T	XP_006719900.1:p.Asp1183Tyr
XM_011535117.3:c.3547G>T	XP_011533419.1:p.Asp1183Tyr
XM_017020627.1:c.3547G>T	XP_016876116.1:p.Asp1183Tyr
NM_000053.4:c.3643G>T MANE Select	NP_000044.2:p.Asp1215Tyr
NM_001005918.3:c.3022G>T	NP_001005918.1:p.Asp1008Tyr
NM_001330579.2:c.3391G>T	NP_001317508.1:p.Asp1131Tyr
NM_001243182.2:c.3310G>T	NP_001230111.1:p.Asp1104Tyr
NM_001330578.2:c.3409G>T	NP_001317507.1:p.Asp1137Tyr