Canonical Allele Identifier: CA1435768536
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291135C= , CM000666.2:g.6291135C= GRCh38
NC_000004.11:g.6292862C= , CM000666.1:g.6292862C= GRCh37
NC_000004.10:g.6343763C= NCBI36
NG_011700.1:g.26286C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.461-62C= ENSP00000507852.1:n.461-62C=
ENST00000683395.1:c.451-62C=
ENST00000684087.1:c.461-62C= ENSP00000506978.1:n.461-62C=
ENST00000684700.1:c.461-62C= ENSP00000507806.1:n.461-62C=
ENST00000506362.2:c.212-62C= ENSP00000424103.2:n.212-62C=
ENST00000673642.1:c.260-62C= ENSP00000501242.1:n.260-62C=
ENST00000673991.1:c.461-62C= ENSP00000501033.1:n.461-62C=
ENST00000674051.1:c.335-62C= ENSP00000501083.1:n.335-62C=
ENST00000226760.5:c.461-62C= MANE Select ENSP00000226760.1:n.461-62C=
ENST00000503569.5:c.461-62C= ENSP00000423337.1:n.461-62C=
ENST00000506362.1:c.58-62C=
ENST00000507765.1:n.646-62C=
NM_001145853.1:c.461-62C= NP_001139325.1:n.461-62C=
NM_006005.3:c.461-62C= MANE Select NP_005996.2:n.461-62C=
XM_017008586.1:c.470-62C= XP_016864075.1:n.470-62C=