Canonical Allele Identifier: CA1435771892

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300633_6300641delinsTCCCACGTA , CM000666.2:g.6300633_6300641delinsTCCCACGTA	GRCh38
NC_000004.11:g.6302360_6302368delinsTCCCACGTA , CM000666.1:g.6302360_6302368delinsTCCCACGTA	GRCh37
NC_000004.10:g.6353261_6353269delinsTCCCACGTA	NCBI36
NG_011700.1:g.35784_35792delinsTCCCACGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-24_898-16delinsTCCCACGTA	ENSP00000507852.1:n.898-24_898-16delinsTCCCACGTA
ENST00000683395.1:c.839-24_839-16delinsTCCCACGTA
ENST00000684087.1:c.862-24_862-16delinsTCCCACGTA	ENSP00000506978.1:n.862-24_862-16delinsTCCCACGTA
ENST00000506362.2:c.613-24_613-16delinsTCCCACGTA	ENSP00000424103.2:n.613-24_613-16delinsTCCCACGTA
ENST00000673642.1:c.661-164_661-156delinsTCCCACGTA	ENSP00000501242.1:n.661-164_661-156delinsTCCCACGTA
ENST00000673991.1:c.898-24_898-16delinsTCCCACGTA	ENSP00000501033.1:n.898-24_898-16delinsTCCCACGTA
ENST00000226760.5:c.862-24_862-16delinsTCCCACGTA MANE Select	ENSP00000226760.1:n.862-24_862-16delinsTCCCACGTA
ENST00000503569.5:c.862-24_862-16delinsTCCCACGTA	ENSP00000423337.1:n.862-24_862-16delinsTCCCACGTA
ENST00000506362.1:c.495-24_495-16delinsTCCCACGTA
ENST00000507765.1:n.1047-24_1047-16delinsTCCCACGTA
ENST00000513395.1:n.420-24_420-16delinsTCCCACGTA
NM_001145853.1:c.862-24_862-16delinsTCCCACGTA	NP_001139325.1:n.862-24_862-16delinsTCCCACGTA
NM_006005.3:c.862-24_862-16delinsTCCCACGTA MANE Select	NP_005996.2:n.862-24_862-16delinsTCCCACGTA
XM_017008586.1:c.871-24_871-16delinsTCCCACGTA	XP_016864075.1:n.871-24_871-16delinsTCCCACGTA