Canonical Allele Identifier: CA375644824

Gene: NOTCH1

Linked Data

• dbSNP Id: rs775109231
• MyVariant Identifiers: chr9:g.139399321G>C (hg19) ; chr9:g.136504869G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504869G>C , CM000671.2:g.136504869G>C	GRCh38
NC_000009.11:g.139399321G>C , CM000671.1:g.139399321G>C	GRCh37
NC_000009.10:g.138519142G>C	NCBI36
NG_007458.1:g.45918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2629C>G
ENST00000651671.1:c.4822C>G MANE Select	ENSP00000498587.1:p.Arg1608Gly
ENST00000679595.1:c.4822C>G	ENSP00000506241.1:p.Arg1608Gly
ENST00000680133.1:c.4708C>G	ENSP00000505319.1:p.Arg1570Gly
ENST00000680218.1:c.4702C>G	ENSP00000505339.1:p.Arg1568Gly
ENST00000680668.1:c.4708C>G	ENSP00000506336.1:p.Arg1570Gly
ENST00000680778.1:c.2419C>G	ENSP00000506033.1:p.Arg807Gly
ENST00000680924.1:c.*2222C>G	ENSP00000506031.1:n.*2222C>G
ENST00000681135.1:c.*2431C>G	ENSP00000506636.1:n.*2431C>G
ENST00000681298.1:n.1635C>G
ENST00000681454.1:c.*4058C>G	ENSP00000505763.1:n.*4058C>G
ENST00000277541.6:c.4822C>G	ENSP00000277541.6:p.Arg1608Gly
NM_017617.3:c.4822C>G	NP_060087.3:p.Arg1608Gly
XM_011518717.1:c.4123C>G	XP_011517019.1:p.Arg1375Gly
NM_017617.5:c.4822C>G MANE Select	NP_060087.3:p.Arg1608Gly
XM_011518717.2:c.4099C>G	XP_011517019.2:p.Arg1367Gly