Canonical Allele Identifier: CA1435773497

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303069_6303072delinsCCTG , CM000666.2:g.6303069_6303072delinsCCTG	GRCh38
NC_000004.11:g.6304796_6304799delinsCCTG , CM000666.1:g.6304796_6304799delinsCCTG	GRCh37
NC_000004.10:g.6355697_6355700delinsCCTG	NCBI36
NG_011700.1:g.38220_38223delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*601_*604delinsCCTG	ENSP00000507852.1:n.*601_*604delinsCCTG
ENST00000683395.1:c.3251_3254delinsCCTG
ENST00000684087.1:c.*601_*604delinsCCTG	ENSP00000506978.1:n.*601_*604delinsCCTG
ENST00000673991.1:c.*601_*604delinsCCTG	ENSP00000501033.1:n.*601_*604delinsCCTG
ENST00000226760.5:c.*601_*604delinsCCTG MANE Select	ENSP00000226760.1:n.*601_*604delinsCCTG
ENST00000507765.1:n.3459_3462delinsCCTG
NM_001145853.1:c.*601_*604delinsCCTG	NP_001139325.1:n.*601_*604delinsCCTG
NM_006005.3:c.*601_*604delinsCCTG MANE Select	NP_005996.2:n.*601_*604delinsCCTG
XM_017008586.1:c.*601_*604delinsCCTG	XP_016864075.1:n.*601_*604delinsCCTG
XR_001741566.2:n.1873_1876delinsCAGG