Canonical Allele Identifier: CA1435772943

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302557_6302576delinsCGCCTGTGCCCACGTGTGCA , CM000666.2:g.6302557_6302576delinsCGCCTGTGCCCACGTGTGCA	GRCh38
NC_000004.11:g.6304284_6304303delinsCGCCTGTGCCCACGTGTGCA , CM000666.1:g.6304284_6304303delinsCGCCTGTGCCCACGTGTGCA	GRCh37
NC_000004.10:g.6355185_6355204delinsCGCCTGTGCCCACGTGTGCA	NCBI36
NG_011700.1:g.37708_37727delinsCGCCTGTGCCCACGTGTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	ENSP00000507852.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000683395.1:c.2739_2758delinsCGCCTGTGCCCACGTGTGCA
ENST00000684087.1:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	ENSP00000506978.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000506362.2:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	ENSP00000424103.2:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000673991.1:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	ENSP00000501033.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000226760.5:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA MANE Select	ENSP00000226760.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000503569.5:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	ENSP00000423337.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
ENST00000507765.1:n.2947_2966delinsCGCCTGTGCCCACGTGTGCA
NM_001145853.1:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	NP_001139325.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
NM_006005.3:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA MANE Select	NP_005996.2:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA
XM_017008586.1:c.*89_*108delinsCGCCTGTGCCCACGTGTGCA	XP_016864075.1:n.*89_*108delinsCGCCTGTGCCCACGTGTGCA