Canonical Allele Identifier: CA1435773458

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303024_6303026delinsAGT , CM000666.2:g.6303024_6303026delinsAGT	GRCh38
NC_000004.11:g.6304751_6304753delinsAGT , CM000666.1:g.6304751_6304753delinsAGT	GRCh37
NC_000004.10:g.6355652_6355654delinsAGT	NCBI36
NG_011700.1:g.38175_38177delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*556_*558delinsAGT	ENSP00000507852.1:n.*556_*558delinsAGT
ENST00000683395.1:c.3206_3208delinsAGT
ENST00000684087.1:c.*556_*558delinsAGT	ENSP00000506978.1:n.*556_*558delinsAGT
ENST00000673991.1:c.*556_*558delinsAGT	ENSP00000501033.1:n.*556_*558delinsAGT
ENST00000226760.5:c.*556_*558delinsAGT MANE Select	ENSP00000226760.1:n.*556_*558delinsAGT
ENST00000507765.1:n.3414_3416delinsAGT
NM_001145853.1:c.*556_*558delinsAGT	NP_001139325.1:n.*556_*558delinsAGT
NM_006005.3:c.*556_*558delinsAGT MANE Select	NP_005996.2:n.*556_*558delinsAGT
XM_017008586.1:c.*556_*558delinsAGT	XP_016864075.1:n.*556_*558delinsAGT
XR_001741566.2:n.1919_1921delinsACT