Canonical Allele Identifier: CA2760283985

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291508_6291509insACA , CM000666.2:g.6291508_6291509insACA	GRCh38
NC_000004.11:g.6293235_6293236insACA , CM000666.1:g.6293235_6293236insACA	GRCh37
NC_000004.10:g.6344136_6344137insACA	NCBI36
NG_011700.1:g.26659_26660insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+141_631+142insACA	ENSP00000507852.1:n.631+141_631+142insACA
ENST00000683395.1:c.608+154_608+155insACA
ENST00000684087.1:c.631+141_631+142insACA	ENSP00000506978.1:n.631+141_631+142insACA
ENST00000684700.1:c.*67_*68insACA	ENSP00000507806.1:n.*67_*68insACA
ENST00000506362.2:c.382+141_382+142insACA	ENSP00000424103.2:n.382+141_382+142insACA
ENST00000673642.1:c.430+141_430+142insACA	ENSP00000501242.1:n.430+141_430+142insACA
ENST00000673991.1:c.631+141_631+142insACA	ENSP00000501033.1:n.631+141_631+142insACA
ENST00000226760.5:c.631+141_631+142insACA MANE Select	ENSP00000226760.1:n.631+141_631+142insACA
ENST00000503569.5:c.631+141_631+142insACA	ENSP00000423337.1:n.631+141_631+142insACA
ENST00000506362.1:c.228+141_228+142insACA
ENST00000507765.1:n.816+141_816+142insACA
NM_001145853.1:c.631+141_631+142insACA	NP_001139325.1:n.631+141_631+142insACA
NM_006005.3:c.631+141_631+142insACA MANE Select	NP_005996.2:n.631+141_631+142insACA
XM_017008586.1:c.640+141_640+142insACA	XP_016864075.1:n.640+141_640+142insACA