Canonical Allele Identifier: CA1435768938

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291903_6291905delinsCCT , CM000666.2:g.6291903_6291905delinsCCT	GRCh38
NC_000004.11:g.6293630_6293632delinsCCT , CM000666.1:g.6293630_6293632delinsCCT	GRCh37
NC_000004.10:g.6344531_6344533delinsCCT	NCBI36
NG_011700.1:g.27054_27056delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-14_632-12delinsCCT	ENSP00000507852.1:n.632-14_632-12delinsCCT
ENST00000683395.1:c.609-14_609-12delinsCCT
ENST00000684087.1:c.632-14_632-12delinsCCT	ENSP00000506978.1:n.632-14_632-12delinsCCT
ENST00000506362.2:c.383-14_383-12delinsCCT	ENSP00000424103.2:n.383-14_383-12delinsCCT
ENST00000673642.1:c.431-14_431-12delinsCCT	ENSP00000501242.1:n.431-14_431-12delinsCCT
ENST00000673991.1:c.632-14_632-12delinsCCT	ENSP00000501033.1:n.632-14_632-12delinsCCT
ENST00000226760.5:c.632-14_632-12delinsCCT MANE Select	ENSP00000226760.1:n.632-14_632-12delinsCCT
ENST00000503569.5:c.632-14_632-12delinsCCT	ENSP00000423337.1:n.632-14_632-12delinsCCT
ENST00000506362.1:c.229-14_229-12delinsCCT
ENST00000507765.1:n.817-14_817-12delinsCCT
NM_001145853.1:c.632-14_632-12delinsCCT	NP_001139325.1:n.632-14_632-12delinsCCT
NM_006005.3:c.632-14_632-12delinsCCT MANE Select	NP_005996.2:n.632-14_632-12delinsCCT
XM_017008586.1:c.641-14_641-12delinsCCT	XP_016864075.1:n.641-14_641-12delinsCCT