Canonical Allele Identifier: CA913107300

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303914_6303944del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302188_6302218del , CM000666.2:g.6302188_6302218del	GRCh38
NC_000004.11:g.6303915_6303945del , CM000666.1:g.6303915_6303945del	GRCh37
NC_000004.10:g.6354816_6354846del	NCBI36
NG_011700.1:g.37339_37369del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2429_2459del	ENSP00000507852.1:p.Val810AlafsTer?
ENST00000683395.1:c.2370_2400del
ENST00000684087.1:c.2393_2423del	ENSP00000506978.1:p.Val798AlafsTer?
ENST00000506362.2:c.2144_2174del	ENSP00000424103.2:p.Val715AlafsTer?
ENST00000673991.1:c.2429_2459del	ENSP00000501033.1:p.Val810AlafsTer?
ENST00000226760.5:c.2393_2423del MANE Select	ENSP00000226760.1:p.Val798AlafsTer?
ENST00000503569.5:c.2393_2423del	ENSP00000423337.1:p.Val798AlafsTer?
ENST00000507765.1:n.2578_2608del
NM_001145853.1:c.2393_2423del	NP_001139325.1:p.Val798AlafsTer?
NM_006005.3:c.2393_2423del MANE Select	NP_005996.2:p.Val798AlafsTer?
XM_017008586.1:c.2402_2432del	XP_016864075.1:p.Val801AlafsTer?