Canonical Allele Identifier: CA2669843895

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302828-TCTTTCTTTTGTGTTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302829_6302844del , CM000666.2:g.6302829_6302844del	GRCh38
NC_000004.11:g.6304556_6304571del , CM000666.1:g.6304556_6304571del	GRCh37
NC_000004.10:g.6355457_6355472del	NCBI36
NG_011700.1:g.37980_37995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*361_*376del	ENSP00000507852.1:n.*361_*376del
ENST00000683395.1:c.3011_3026del
ENST00000684087.1:c.*361_*376del	ENSP00000506978.1:n.*361_*376del
ENST00000506362.2:c.*361_*376del	ENSP00000424103.2:n.*361_*376del
ENST00000673991.1:c.*361_*376del	ENSP00000501033.1:n.*361_*376del
ENST00000226760.5:c.*361_*376del MANE Select	ENSP00000226760.1:n.*361_*376del
ENST00000503569.5:c.*361_*376del	ENSP00000423337.1:n.*361_*376del
ENST00000507765.1:n.3219_3234del
NM_001145853.1:c.*361_*376del	NP_001139325.1:n.*361_*376del
NM_006005.3:c.*361_*376del MANE Select	NP_005996.2:n.*361_*376del
XM_017008586.1:c.*361_*376del	XP_016864075.1:n.*361_*376del