Canonical Allele Identifier: CA2645384357

Gene: TOE1

Linked Data

• gnomAD v4: 1-45341459-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341459T>C , CM000663.2:g.45341459T>C	GRCh38
NC_000001.10:g.45807131T>C , CM000663.1:g.45807131T>C	GRCh37
NC_000001.9:g.45579718T>C	NCBI36
NG_008189.1:g.4012A>G , LRG_220:g.4012A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.237-14T>C MANE Select	ENSP00000361162.5:n.237-14T>C
ENST00000671898.1:c.541-6948A>G	ENSP00000499896.1:n.541-6948A>G
ENST00000372090.5:c.237-14T>C	ENSP00000361162.5:n.237-14T>C
ENST00000460057.1:n.48+116T>C
ENST00000471337.5:n.315-14T>C
ENST00000477731.5:n.456-14T>C
ENST00000495703.5:n.507-14T>C
NM_025077.3:c.237-14T>C	NP_079353.3:n.237-14T>C
XM_005270412.2:c.255-14T>C	XP_005270469.1:n.255-14T>C
XM_005270413.3:c.99-14T>C	XP_005270470.1:n.99-14T>C
XM_011540569.1:c.-49+116T>C	XP_011538871.1:n.-49+116T>C
XR_246230.2:n.514-14T>C
XR_426587.2:n.334-14T>C
XR_946532.1:n.334-14T>C
XM_005270412.4:c.255-14T>C	XP_005270469.1:n.255-14T>C
XM_005270413.5:c.99-14T>C	XP_005270470.1:n.99-14T>C
XM_011540569.3:c.-49+116T>C	XP_011538871.1:n.-49+116T>C
XM_024452837.1:c.186-14T>C	XP_024308605.1:n.186-14T>C
XR_001736951.2:n.424-14T>C
XR_002959287.1:n.826-14T>C
XR_246230.4:n.424-14T>C
XR_426587.4:n.334-14T>C
XR_946532.3:n.334-14T>C
NM_025077.4:c.237-14T>C MANE Select	NP_079353.3:n.237-14T>C