Canonical Allele Identifier: CA523341550

Gene: WLS GNG12-AS1

Linked Data

• dbSNP Id: rs1017074960
• gnomAD v2: 1-68635096-G-A
• gnomAD v3: 1-68169413-G-A
• gnomAD v4: 1-68169413-G-A
• MyVariant Identifiers: chr1:g.68635096G>A (hg19) ; chr1:g.68169413G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.68169413G>A , CM000663.2:g.68169413G>A	GRCh38
NC_000001.10:g.68635096G>A , CM000663.1:g.68635096G>A	GRCh37
NC_000001.9:g.68407684G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262348.9:c.380-10166C>T (WLS) MANE Select	ENSP00000262348.4:n.380-10166C>T
ENST00000262348.8:c.380-10166C>T (WLS)	ENSP00000262348.4:n.380-10166C>T
ENST00000354777.6:c.374-10166C>T (WLS)	ENSP00000346829.2:n.374-10166C>T
ENST00000370973.2:c.-20-10166C>T (WLS)	ENSP00000360012.2:n.-20-10166C>T
ENST00000370976.7:c.107-10166C>T (WLS)	ENSP00000360015.3:n.107-10166C>T
ENST00000471243.2:c.245-10166C>T (WLS)	ENSP00000436196.1:n.245-10166C>T
ENST00000491076.1:c.*298-10166C>T (WLS)	ENSP00000433188.1:n.*298-10166C>T
ENST00000497187.5:n.60+6905C>T (WLS)
ENST00000527864.1:c.507-10166C>T (WLS)
ENST00000530486.5:c.245-10166C>T (WLS)	ENSP00000433111.1:n.245-10166C>T
ENST00000533537.5:c.-20-10166C>T (WLS)	ENSP00000433690.1:n.-20-10166C>T
ENST00000534713.5:c.88-10166C>T (WLS)
NM_001002292.3:c.374-10166C>T (WLS)	NP_001002292.3:n.374-10166C>T
NM_001193334.1:c.107-10166C>T (WLS)	NP_001180263.1:n.107-10166C>T
NM_024911.6:c.380-10166C>T (WLS)	NP_079187.3:n.380-10166C>T
NR_040077.1:n.1228+30963G>A (GNG12-AS1)
XM_011542191.1:c.380-10166C>T (WLS)	XP_011540493.1:n.380-10166C>T
XM_011542192.1:c.245-10166C>T (WLS)	XP_011540494.1:n.245-10166C>T
XM_011542191.2:c.380-10166C>T (WLS)	XP_011540493.1:n.380-10166C>T
XM_011542192.3:c.245-10166C>T (WLS)	XP_011540494.1:n.245-10166C>T
XM_017002390.2:c.245-10166C>T (WLS)	XP_016857879.1:n.245-10166C>T
NM_024911.7:c.380-10166C>T (WLS) MANE Select	NP_079187.3:n.380-10166C>T
NM_001002292.4:c.374-10166C>T (WLS)	NP_001002292.3:n.374-10166C>T