Canonical Allele Identifier: CA522810590

Gene: TOE1

Linked Data

• dbSNP Id: rs1211937199
• gnomAD v2: 1-45807121-GC-G
• gnomAD v4: 1-45341449-GC-G
• MyVariant Identifiers: chr1:g.45807122del (hg19) ; chr1:g.45341450del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341450del , CM000663.2:g.45341450del	GRCh38
NC_000001.10:g.45807122del , CM000663.1:g.45807122del	GRCh37
NC_000001.9:g.45579709del	NCBI36
NG_008189.1:g.4021del , LRG_220:g.4021del

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.237-23del MANE Select	ENSP00000361162.5:n.237-23del
ENST00000671898.1:c.541-6939del	ENSP00000499896.1:n.541-6939del
ENST00000372090.5:c.237-23del	ENSP00000361162.5:n.237-23del
ENST00000460057.1:n.48+107del
ENST00000471337.5:n.315-23del
ENST00000477731.5:n.456-23del
ENST00000495703.5:n.507-23del
NM_025077.3:c.237-23del	NP_079353.3:n.237-23del
XM_005270412.2:c.255-23del	XP_005270469.1:n.255-23del
XM_005270413.3:c.99-23del	XP_005270470.1:n.99-23del
XM_011540569.1:c.-49+107del	XP_011538871.1:n.-49+107del
XR_246230.2:n.514-23del
XR_426587.2:n.334-23del
XR_946532.1:n.334-23del
XM_005270412.4:c.255-23del	XP_005270469.1:n.255-23del
XM_005270413.5:c.99-23del	XP_005270470.1:n.99-23del
XM_011540569.3:c.-49+107del	XP_011538871.1:n.-49+107del
XM_024452837.1:c.186-23del	XP_024308605.1:n.186-23del
XR_001736951.2:n.424-23del
XR_002959287.1:n.826-23del
XR_246230.4:n.424-23del
XR_426587.4:n.334-23del
XR_946532.3:n.334-23del
NM_025077.4:c.237-23del MANE Select	NP_079353.3:n.237-23del