Canonical Allele Identifier: CA1001248920

Gene: TOE1

Linked Data

• dbSNP Id: rs1646911937
• gnomAD v3: 1-45340904-A-G
• gnomAD v4: 1-45340904-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45340904A>G , CM000663.2:g.45340904A>G	GRCh38
NC_000001.10:g.45806576A>G , CM000663.1:g.45806576A>G	GRCh37
NC_000001.9:g.45579163A>G	NCBI36
NG_008189.1:g.4567T>C , LRG_220:g.4567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372090.6:c.53-169A>G MANE Select	ENSP00000361162.5:n.53-169A>G
ENST00000671898.1:c.541-6393T>C	ENSP00000499896.1:n.541-6393T>C
ENST00000372090.5:c.53-169A>G	ENSP00000361162.5:n.53-169A>G
ENST00000471337.5:n.131-169A>G
ENST00000477731.5:n.272-169A>G
ENST00000495703.5:n.323-169A>G
NM_025077.3:c.53-169A>G	NP_079353.3:n.53-169A>G
XM_005270412.2:c.71-169A>G	XP_005270469.1:n.71-169A>G
XM_005270413.3:c.-86-169A>G	XP_005270470.1:n.-86-169A>G
XM_011540569.1:c.-232-169A>G	XP_011538871.1:n.-232-169A>G
XR_246230.2:n.330-169A>G
XR_426587.2:n.150-169A>G
XR_946532.1:n.150-169A>G
XM_005270412.4:c.71-169A>G	XP_005270469.1:n.71-169A>G
XM_005270413.5:c.-86-169A>G	XP_005270470.1:n.-86-169A>G
XM_011540569.3:c.-232-169A>G	XP_011538871.1:n.-232-169A>G
XM_024452837.1:c.-86-169A>G	XP_024308605.1:n.-86-169A>G
XR_001736951.2:n.240-169A>G
XR_002959287.1:n.555-169A>G
XR_246230.4:n.240-169A>G
XR_426587.4:n.150-169A>G
XR_946532.3:n.150-169A>G
NM_025077.4:c.53-169A>G MANE Select	NP_079353.3:n.53-169A>G