Canonical Allele Identifier: CA1435771634

Gene: WFS1

Linked Data

• dbSNP Id: rs1730835382

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300418_6300424del , CM000666.2:g.6300418_6300424del	GRCh38
NC_000004.11:g.6302145_6302151del , CM000666.1:g.6302145_6302151del	GRCh37
NC_000004.10:g.6353046_6353052del	NCBI36
NG_011700.1:g.35569_35575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-239_898-233del	ENSP00000507852.1:n.898-239_898-233del
ENST00000683395.1:c.839-239_839-233del
ENST00000684087.1:c.862-239_862-233del	ENSP00000506978.1:n.862-239_862-233del
ENST00000506362.2:c.613-239_613-233del	ENSP00000424103.2:n.613-239_613-233del
ENST00000673642.1:c.661-379_661-373del	ENSP00000501242.1:n.661-379_661-373del
ENST00000673991.1:c.898-239_898-233del	ENSP00000501033.1:n.898-239_898-233del
ENST00000226760.5:c.862-239_862-233del MANE Select	ENSP00000226760.1:n.862-239_862-233del
ENST00000503569.5:c.862-239_862-233del	ENSP00000423337.1:n.862-239_862-233del
ENST00000506362.1:c.495-239_495-233del
ENST00000507765.1:n.1047-239_1047-233del
ENST00000513395.1:n.420-239_420-233del
NM_001145853.1:c.862-239_862-233del	NP_001139325.1:n.862-239_862-233del
NM_006005.3:c.862-239_862-233del MANE Select	NP_005996.2:n.862-239_862-233del
XM_017008586.1:c.871-239_871-233del	XP_016864075.1:n.871-239_871-233del