Canonical Allele Identifier: CA1435771859

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300610_6300611delinsTG , CM000666.2:g.6300610_6300611delinsTG	GRCh38
NC_000004.11:g.6302337_6302338delinsTG , CM000666.1:g.6302337_6302338delinsTG	GRCh37
NC_000004.10:g.6353238_6353239delinsTG	NCBI36
NG_011700.1:g.35761_35762delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-47_898-46delinsTG	ENSP00000507852.1:n.898-47_898-46delinsTG
ENST00000683395.1:c.839-47_839-46delinsTG
ENST00000684087.1:c.862-47_862-46delinsTG	ENSP00000506978.1:n.862-47_862-46delinsTG
ENST00000506362.2:c.613-47_613-46delinsTG	ENSP00000424103.2:n.613-47_613-46delinsTG
ENST00000673642.1:c.661-187_661-186delinsTG	ENSP00000501242.1:n.661-187_661-186delinsTG
ENST00000673991.1:c.898-47_898-46delinsTG	ENSP00000501033.1:n.898-47_898-46delinsTG
ENST00000226760.5:c.862-47_862-46delinsTG MANE Select	ENSP00000226760.1:n.862-47_862-46delinsTG
ENST00000503569.5:c.862-47_862-46delinsTG	ENSP00000423337.1:n.862-47_862-46delinsTG
ENST00000506362.1:c.495-47_495-46delinsTG
ENST00000507765.1:n.1047-47_1047-46delinsTG
ENST00000513395.1:n.420-47_420-46delinsTG
NM_001145853.1:c.862-47_862-46delinsTG	NP_001139325.1:n.862-47_862-46delinsTG
NM_006005.3:c.862-47_862-46delinsTG MANE Select	NP_005996.2:n.862-47_862-46delinsTG
XM_017008586.1:c.871-47_871-46delinsTG	XP_016864075.1:n.871-47_871-46delinsTG