Canonical Allele Identifier: CA1435773211

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302797_6302800delinsTCCC , CM000666.2:g.6302797_6302800delinsTCCC	GRCh38
NC_000004.11:g.6304524_6304527delinsTCCC , CM000666.1:g.6304524_6304527delinsTCCC	GRCh37
NC_000004.10:g.6355425_6355428delinsTCCC	NCBI36
NG_011700.1:g.37948_37951delinsTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*329_*332delinsTCCC	ENSP00000507852.1:n.*329_*332delinsTCCC
ENST00000683395.1:c.2979_2982delinsTCCC
ENST00000684087.1:c.*329_*332delinsTCCC	ENSP00000506978.1:n.*329_*332delinsTCCC
ENST00000506362.2:c.*329_*332delinsTCCC	ENSP00000424103.2:n.*329_*332delinsTCCC
ENST00000673991.1:c.*329_*332delinsTCCC	ENSP00000501033.1:n.*329_*332delinsTCCC
ENST00000226760.5:c.*329_*332delinsTCCC MANE Select	ENSP00000226760.1:n.*329_*332delinsTCCC
ENST00000503569.5:c.*329_*332delinsTCCC	ENSP00000423337.1:n.*329_*332delinsTCCC
ENST00000507765.1:n.3187_3190delinsTCCC
NM_001145853.1:c.*329_*332delinsTCCC	NP_001139325.1:n.*329_*332delinsTCCC
NM_006005.3:c.*329_*332delinsTCCC MANE Select	NP_005996.2:n.*329_*332delinsTCCC
XM_017008586.1:c.*329_*332delinsTCCC	XP_016864075.1:n.*329_*332delinsTCCC