Canonical Allele Identifier: CA2760284543

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300451A>C , CM000666.2:g.6300451A>C	GRCh38
NC_000004.11:g.6302178A>C , CM000666.1:g.6302178A>C	GRCh37
NC_000004.10:g.6353079A>C	NCBI36
NG_011700.1:g.35602A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-206A>C	ENSP00000507852.1:n.898-206A>C
ENST00000683395.1:c.839-206A>C
ENST00000684087.1:c.862-206A>C	ENSP00000506978.1:n.862-206A>C
ENST00000506362.2:c.613-206A>C	ENSP00000424103.2:n.613-206A>C
ENST00000673642.1:c.661-346A>C	ENSP00000501242.1:n.661-346A>C
ENST00000673991.1:c.898-206A>C	ENSP00000501033.1:n.898-206A>C
ENST00000226760.5:c.862-206A>C MANE Select	ENSP00000226760.1:n.862-206A>C
ENST00000503569.5:c.862-206A>C	ENSP00000423337.1:n.862-206A>C
ENST00000506362.1:c.495-206A>C
ENST00000507765.1:n.1047-206A>C
ENST00000513395.1:n.420-206A>C
NM_001145853.1:c.862-206A>C	NP_001139325.1:n.862-206A>C
NM_006005.3:c.862-206A>C MANE Select	NP_005996.2:n.862-206A>C
XM_017008586.1:c.871-206A>C	XP_016864075.1:n.871-206A>C