Canonical Allele Identifier: CA1435771889

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300631_6300647delinsGTTCCCACGTACCATCT , CM000666.2:g.6300631_6300647delinsGTTCCCACGTACCATCT	GRCh38
NC_000004.11:g.6302358_6302374delinsGTTCCCACGTACCATCT , CM000666.1:g.6302358_6302374delinsGTTCCCACGTACCATCT	GRCh37
NC_000004.10:g.6353259_6353275delinsGTTCCCACGTACCATCT	NCBI36
NG_011700.1:g.35782_35798delinsGTTCCCACGTACCATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-26_898-10delinsGTTCCCACGTACCATCT	ENSP00000507852.1:n.898-26_898-10delinsGTTCCCACGTACCATCT
ENST00000683395.1:c.839-26_839-10delinsGTTCCCACGTACCATCT
ENST00000684087.1:c.862-26_862-10delinsGTTCCCACGTACCATCT	ENSP00000506978.1:n.862-26_862-10delinsGTTCCCACGTACCATCT
ENST00000506362.2:c.613-26_613-10delinsGTTCCCACGTACCATCT	ENSP00000424103.2:n.613-26_613-10delinsGTTCCCACGTACCATCT
ENST00000673642.1:c.661-166_661-150delinsGTTCCCACGTACCATCT	ENSP00000501242.1:n.661-166_661-150delinsGTTCCCACGTACCATCT
ENST00000673991.1:c.898-26_898-10delinsGTTCCCACGTACCATCT	ENSP00000501033.1:n.898-26_898-10delinsGTTCCCACGTACCATCT
ENST00000226760.5:c.862-26_862-10delinsGTTCCCACGTACCATCT MANE Select	ENSP00000226760.1:n.862-26_862-10delinsGTTCCCACGTACCATCT
ENST00000503569.5:c.862-26_862-10delinsGTTCCCACGTACCATCT	ENSP00000423337.1:n.862-26_862-10delinsGTTCCCACGTACCATCT
ENST00000506362.1:c.495-26_495-10delinsGTTCCCACGTACCATCT
ENST00000507765.1:n.1047-26_1047-10delinsGTTCCCACGTACCATCT
ENST00000513395.1:n.420-26_420-10delinsGTTCCCACGTACCATCT
NM_001145853.1:c.862-26_862-10delinsGTTCCCACGTACCATCT	NP_001139325.1:n.862-26_862-10delinsGTTCCCACGTACCATCT
NM_006005.3:c.862-26_862-10delinsGTTCCCACGTACCATCT MANE Select	NP_005996.2:n.862-26_862-10delinsGTTCCCACGTACCATCT
XM_017008586.1:c.871-26_871-10delinsGTTCCCACGTACCATCT	XP_016864075.1:n.871-26_871-10delinsGTTCCCACGTACCATCT