Canonical Allele Identifier: CA1435771648

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300431_6300432delinsAG , CM000666.2:g.6300431_6300432delinsAG	GRCh38
NC_000004.11:g.6302158_6302159delinsAG , CM000666.1:g.6302158_6302159delinsAG	GRCh37
NC_000004.10:g.6353059_6353060delinsAG	NCBI36
NG_011700.1:g.35582_35583delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-226_898-225delinsAG	ENSP00000507852.1:n.898-226_898-225delinsAG
ENST00000683395.1:c.839-226_839-225delinsAG
ENST00000684087.1:c.862-226_862-225delinsAG	ENSP00000506978.1:n.862-226_862-225delinsAG
ENST00000506362.2:c.613-226_613-225delinsAG	ENSP00000424103.2:n.613-226_613-225delinsAG
ENST00000673642.1:c.661-366_661-365delinsAG	ENSP00000501242.1:n.661-366_661-365delinsAG
ENST00000673991.1:c.898-226_898-225delinsAG	ENSP00000501033.1:n.898-226_898-225delinsAG
ENST00000226760.5:c.862-226_862-225delinsAG MANE Select	ENSP00000226760.1:n.862-226_862-225delinsAG
ENST00000503569.5:c.862-226_862-225delinsAG	ENSP00000423337.1:n.862-226_862-225delinsAG
ENST00000506362.1:c.495-226_495-225delinsAG
ENST00000507765.1:n.1047-226_1047-225delinsAG
ENST00000513395.1:n.420-226_420-225delinsAG
NM_001145853.1:c.862-226_862-225delinsAG	NP_001139325.1:n.862-226_862-225delinsAG
NM_006005.3:c.862-226_862-225delinsAG MANE Select	NP_005996.2:n.862-226_862-225delinsAG
XM_017008586.1:c.871-226_871-225delinsAG	XP_016864075.1:n.871-226_871-225delinsAG