Canonical Allele Identifier: CA736163171

Gene: TOE1 MUTYH

Linked Data

• dbSNP Id: rs1163162966
• gnomAD v3: 1-45340795-C-G
• gnomAD v4: 1-45340795-C-G
• MyVariant Identifiers: chr1:g.45806467C>G (hg19) ; chr1:g.45340795C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45340795C>G , CM000663.2:g.45340795C>G	GRCh38
NC_000001.10:g.45806467C>G , CM000663.1:g.45806467C>G	GRCh37
NC_000001.9:g.45579054C>G	NCBI36
NG_008189.1:g.4676G>C , LRG_220:g.4676G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.53-278C>G (TOE1) MANE Select	ENSP00000361162.5:n.53-278C>G
ENST00000671898.1:c.541-6284G>C	ENSP00000499896.1:n.541-6284G>C
ENST00000672011.1:c.-541G>C (MUTYH)	ENSP00000500418.1:n.-541G>C
ENST00000372090.5:c.53-278C>G (TOE1)	ENSP00000361162.5:n.53-278C>G
ENST00000471337.5:n.131-278C>G (TOE1)
ENST00000477731.5:n.272-278C>G (TOE1)
ENST00000495703.5:n.322+253C>G (TOE1)
NM_025077.3:c.53-278C>G (TOE1)	NP_079353.3:n.53-278C>G
XM_005270412.2:c.71-278C>G (TOE1)	XP_005270469.1:n.71-278C>G
XM_005270413.3:c.-87+253C>G (TOE1)	XP_005270470.1:n.-87+253C>G
XM_011540569.1:c.-232-278C>G (TOE1)	XP_011538871.1:n.-232-278C>G
XR_246230.2:n.330-278C>G (TOE1)
XR_426587.2:n.150-278C>G (TOE1)
XR_946532.1:n.150-278C>G (TOE1)
XM_005270412.4:c.71-278C>G (TOE1)	XP_005270469.1:n.71-278C>G
XM_005270413.5:c.-87+253C>G (TOE1)	XP_005270470.1:n.-87+253C>G
XM_011540569.3:c.-232-278C>G (TOE1)	XP_011538871.1:n.-232-278C>G
XM_024452837.1:c.-87+253C>G (TOE1)	XP_024308605.1:n.-87+253C>G
XR_001736951.2:n.240-278C>G (TOE1)
XR_002959287.1:n.555-278C>G (TOE1)
XR_246230.4:n.240-278C>G (TOE1)
XR_426587.4:n.150-278C>G (TOE1)
XR_946532.3:n.150-278C>G (TOE1)
NM_025077.4:c.53-278C>G (TOE1) MANE Select	NP_079353.3:n.53-278C>G