Canonical Allele Identifier: CA738137032

Gene: WLS GNG12-AS1

Linked Data

• dbSNP Id: rs770433237
• gnomAD v3: 1-68191879-G-A
• gnomAD v4: 1-68191879-G-A
• MyVariant Identifiers: chr1:g.68657562G>A (hg19) ; chr1:g.68191879G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.68191879G>A , CM000663.2:g.68191879G>A	GRCh38
NC_000001.10:g.68657562G>A , CM000663.1:g.68657562G>A	GRCh37
NC_000001.9:g.68430150G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262348.9:c.379+2076C>T (WLS) MANE Select	ENSP00000262348.4:n.379+2076C>T
ENST00000262348.8:c.379+2076C>T (WLS)	ENSP00000262348.4:n.379+2076C>T
ENST00000354777.6:c.373+2076C>T (WLS)	ENSP00000346829.2:n.373+2076C>T
ENST00000370973.2:c.-21+2076C>T (WLS)	ENSP00000360012.2:n.-21+2076C>T
ENST00000370976.7:c.107-32632C>T (WLS)	ENSP00000360015.3:n.107-32632C>T
ENST00000471243.2:c.244+2076C>T (WLS)	ENSP00000436196.1:n.244+2076C>T
ENST00000491076.1:c.*297+2076C>T (WLS)	ENSP00000433188.1:n.*297+2076C>T
ENST00000527864.1:c.396+2076C>T (WLS)
ENST00000530486.5:c.244+2076C>T (WLS)	ENSP00000433111.1:n.244+2076C>T
ENST00000533537.5:c.-20-32632C>T (WLS)	ENSP00000433690.1:n.-20-32632C>T
ENST00000534713.5:c.88-32632C>T (WLS)
NM_001002292.3:c.373+2076C>T (WLS)	NP_001002292.3:n.373+2076C>T
NM_001193334.1:c.107-32632C>T (WLS)	NP_001180263.1:n.107-32632C>T
NM_024911.6:c.379+2076C>T (WLS)	NP_079187.3:n.379+2076C>T
NR_040077.1:n.1229-10090G>A (GNG12-AS1)
XM_011542191.1:c.379+2076C>T (WLS)	XP_011540493.1:n.379+2076C>T
XM_011542192.1:c.244+2076C>T (WLS)	XP_011540494.1:n.244+2076C>T
XM_011542191.2:c.379+2076C>T (WLS)	XP_011540493.1:n.379+2076C>T
XM_011542192.3:c.244+2076C>T (WLS)	XP_011540494.1:n.244+2076C>T
XM_017002390.2:c.244+2076C>T (WLS)	XP_016857879.1:n.244+2076C>T
NM_024911.7:c.379+2076C>T (WLS) MANE Select	NP_079187.3:n.379+2076C>T
NM_001002292.4:c.373+2076C>T (WLS)	NP_001002292.3:n.373+2076C>T