Canonical Allele Identifier: CA1435772414
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300931A= , CM000666.2:g.6300931A= GRCh38
NC_000004.11:g.6302658A= , CM000666.1:g.6302658A= GRCh37
NC_000004.10:g.6353559A= NCBI36
NG_011700.1:g.36082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1172A= ENSP00000507852.1:p.Asp391=
ENST00000683395.1:c.1113A=
ENST00000684087.1:c.1136A= ENSP00000506978.1:p.Asp379=
ENST00000506362.2:c.887A= ENSP00000424103.2:p.Asp296=
ENST00000673642.1:c.795A= ENSP00000501242.1:p.Arg265=
ENST00000673991.1:c.1172A= ENSP00000501033.1:p.Asp391=
ENST00000226760.5:c.1136A= MANE Select ENSP00000226760.1:p.Asp379=
ENST00000503569.5:c.1136A= ENSP00000423337.1:p.Asp379=
ENST00000507765.1:n.1321A=
NM_001145853.1:c.1136A= NP_001139325.1:p.Asp379=
NM_006005.3:c.1136A= MANE Select NP_005996.2:p.Asp379=
XM_017008586.1:c.1145A= XP_016864075.1:p.Asp382=