Canonical Allele Identifier: CA736163017

Gene: TOE1 MUTYH

Linked Data

• dbSNP Id: rs1370783231
• gnomAD v4: 1-45340523-G-A
• MyVariant Identifiers: chr1:g.45806195G>A (hg19) ; chr1:g.45340523G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45340523G>A , CM000663.2:g.45340523G>A	GRCh38
NC_000001.10:g.45806195G>A , CM000663.1:g.45806195G>A	GRCh37
NC_000001.9:g.45578782G>A	NCBI36
NG_008189.1:g.4948C>T , LRG_220:g.4948C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372090.6:c.52+219G>A (TOE1) MANE Select	ENSP00000361162.5:n.52+219G>A
ENST00000671898.1:c.541-6012C>T	ENSP00000499896.1:n.541-6012C>T
ENST00000672011.1:c.-269C>T (MUTYH)	ENSP00000500418.1:n.-269C>T
ENST00000372090.5:c.52+219G>A (TOE1)	ENSP00000361162.5:n.52+219G>A
ENST00000471337.5:n.130+219G>A (TOE1)
ENST00000477731.5:n.271+201G>A (TOE1)
ENST00000495703.5:n.303G>A (TOE1)
NM_025077.3:c.52+219G>A (TOE1)	NP_079353.3:n.52+219G>A
XM_005270412.2:c.70+201G>A (TOE1)	XP_005270469.1:n.70+201G>A
XM_005270413.3:c.-106G>A (TOE1)	XP_005270470.1:n.-106G>A
XM_011540569.1:c.-233+219G>A (TOE1)	XP_011538871.1:n.-233+219G>A
XR_246230.2:n.329+219G>A (TOE1)
XR_426587.2:n.149+201G>A (TOE1)
XR_946532.1:n.149+201G>A (TOE1)
XM_005270412.4:c.70+201G>A (TOE1)	XP_005270469.1:n.70+201G>A
XM_005270413.5:c.-106G>A (TOE1)	XP_005270470.1:n.-106G>A
XM_011540569.3:c.-233+219G>A (TOE1)	XP_011538871.1:n.-233+219G>A
XM_024452837.1:c.-106G>A (TOE1)	XP_024308605.1:n.-106G>A
XR_001736951.2:n.239+219G>A (TOE1)
XR_002959287.1:n.554+219G>A (TOE1)
XR_246230.4:n.239+219G>A (TOE1)
XR_426587.4:n.149+201G>A (TOE1)
XR_946532.3:n.149+201G>A (TOE1)
NM_025077.4:c.52+219G>A (TOE1) MANE Select	NP_079353.3:n.52+219G>A