Canonical Allele Identifier: CA21847838

Gene: TOE1

Linked Data

• dbSNP Id: rs961595649
• MyVariant Identifiers: chr1:g.45806579C>T (hg19) ; chr1:g.45340907C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45340907C>T , CM000663.2:g.45340907C>T	GRCh38
NC_000001.10:g.45806579C>T , CM000663.1:g.45806579C>T	GRCh37
NC_000001.9:g.45579166C>T	NCBI36
NG_008189.1:g.4564G>A , LRG_220:g.4564G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372090.6:c.53-166C>T MANE Select	ENSP00000361162.5:n.53-166C>T
ENST00000671898.1:c.541-6396G>A	ENSP00000499896.1:n.541-6396G>A
ENST00000372090.5:c.53-166C>T	ENSP00000361162.5:n.53-166C>T
ENST00000471337.5:n.131-166C>T
ENST00000477731.5:n.272-166C>T
ENST00000495703.5:n.323-166C>T
NM_025077.3:c.53-166C>T	NP_079353.3:n.53-166C>T
XM_005270412.2:c.71-166C>T	XP_005270469.1:n.71-166C>T
XM_005270413.3:c.-86-166C>T	XP_005270470.1:n.-86-166C>T
XM_011540569.1:c.-232-166C>T	XP_011538871.1:n.-232-166C>T
XR_246230.2:n.330-166C>T
XR_426587.2:n.150-166C>T
XR_946532.1:n.150-166C>T
XM_005270412.4:c.71-166C>T	XP_005270469.1:n.71-166C>T
XM_005270413.5:c.-86-166C>T	XP_005270470.1:n.-86-166C>T
XM_011540569.3:c.-232-166C>T	XP_011538871.1:n.-232-166C>T
XM_024452837.1:c.-86-166C>T	XP_024308605.1:n.-86-166C>T
XR_001736951.2:n.240-166C>T
XR_002959287.1:n.555-166C>T
XR_246230.4:n.240-166C>T
XR_426587.4:n.150-166C>T
XR_946532.3:n.150-166C>T
NM_025077.4:c.53-166C>T MANE Select	NP_079353.3:n.53-166C>T