Canonical Allele Identifier: CA340138741

Gene: TOE1

Linked Data

• MyVariant Identifiers: chr1:g.45807144G>A (hg19) ; chr1:g.45341472G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341472G>A , CM000663.2:g.45341472G>A	GRCh38
NC_000001.10:g.45807144G>A , CM000663.1:g.45807144G>A	GRCh37
NC_000001.9:g.45579731G>A	NCBI36
NG_008189.1:g.3999C>T , LRG_220:g.3999C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.237-1G>A MANE Select	ENSP00000361162.5:n.237-1G>A
ENST00000671898.1:c.541-6961C>T	ENSP00000499896.1:n.541-6961C>T
ENST00000372090.5:c.237-1G>A	ENSP00000361162.5:n.237-1G>A
ENST00000460057.1:n.48+129G>A
ENST00000471337.5:n.315-1G>A
ENST00000477731.5:n.456-1G>A
ENST00000495703.5:n.507-1G>A
NM_025077.3:c.237-1G>A	NP_079353.3:n.237-1G>A
XM_005270412.2:c.255-1G>A	XP_005270469.1:n.255-1G>A
XM_005270413.3:c.99-1G>A	XP_005270470.1:n.99-1G>A
XM_011540569.1:c.-49+129G>A	XP_011538871.1:n.-49+129G>A
XR_246230.2:n.514-1G>A
XR_426587.2:n.334-1G>A
XR_946532.1:n.334-1G>A
XM_005270412.4:c.255-1G>A	XP_005270469.1:n.255-1G>A
XM_005270413.5:c.99-1G>A	XP_005270470.1:n.99-1G>A
XM_011540569.3:c.-49+129G>A	XP_011538871.1:n.-49+129G>A
XM_024452837.1:c.186-1G>A	XP_024308605.1:n.186-1G>A
XR_001736951.2:n.424-1G>A
XR_002959287.1:n.826-1G>A
XR_246230.4:n.424-1G>A
XR_426587.4:n.334-1G>A
XR_946532.3:n.334-1G>A
NM_025077.4:c.237-1G>A MANE Select	NP_079353.3:n.237-1G>A