Canonical Allele Identifier: CA901594

Gene: WLS GNG12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.68137800T>C , CM000663.2:g.68137800T>C	GRCh38
NC_000001.10:g.68603483T>C , CM000663.1:g.68603483T>C	GRCh37
NC_000001.9:g.68376071T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262348.9:c.1496A>G (WLS) MANE Select	ENSP00000262348.4:p.Tyr499Cys
ENST00000262348.8:c.1496A>G (WLS)	ENSP00000262348.4:p.Tyr499Cys
ENST00000354777.6:c.1490A>G (WLS)	ENSP00000346829.2:p.Tyr497Cys
ENST00000370976.7:c.1223A>G (WLS)	ENSP00000360015.3:p.Tyr408Cys
ENST00000498615.1:n.363A>G (WLS)
NM_001002292.3:c.1490A>G (WLS)	NP_001002292.3:p.Tyr497Cys
NM_001193334.1:c.1223A>G (WLS)	NP_001180263.1:p.Tyr408Cys
NM_024911.6:c.1496A>G (WLS)	NP_079187.3:p.Tyr499Cys
NR_040077.1:n.1075-497T>C (GNG12-AS1)
XM_011542191.1:c.1496A>G (WLS)	XP_011540493.1:p.Tyr499Cys
XM_011542192.1:c.1361A>G (WLS)	XP_011540494.1:p.Tyr454Cys
XM_011542191.2:c.1496A>G (WLS)	XP_011540493.1:p.Tyr499Cys
XM_011542192.3:c.1361A>G (WLS)	XP_011540494.1:p.Tyr454Cys
XM_017002390.2:c.1361A>G (WLS)	XP_016857879.1:p.Tyr454Cys
NM_024911.7:c.1496A>G (WLS) MANE Select	NP_079187.3:p.Tyr499Cys
NM_001002292.4:c.1490A>G (WLS)	NP_001002292.3:p.Tyr497Cys