Canonical Allele Identifier: CA375563089

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133368603
• MyVariant Identifiers: chr9:g.139412287A>G (hg19) ; chr9:g.136517835A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136517835A>G , CM000671.2:g.136517835A>G	GRCh38
NC_000009.11:g.139412287A>G , CM000671.1:g.139412287A>G	GRCh37
NC_000009.10:g.138532108A>G	NCBI36
NG_007458.1:g.32952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.1358T>C MANE Select	ENSP00000498587.1:p.Val453Ala
ENST00000679595.1:c.1358T>C	ENSP00000506241.1:p.Val453Ala
ENST00000680133.1:c.1358T>C	ENSP00000505319.1:p.Val453Ala
ENST00000680218.1:c.1358T>C	ENSP00000505339.1:p.Val453Ala
ENST00000680668.1:c.1358T>C	ENSP00000506336.1:p.Val453Ala
ENST00000680924.1:c.1358T>C	ENSP00000506031.1:p.Val453Ala
ENST00000681135.1:c.1358T>C	ENSP00000506636.1:p.Val453Ala
ENST00000681454.1:c.*594T>C	ENSP00000505763.1:n.*594T>C
ENST00000277541.6:c.1358T>C	ENSP00000277541.6:p.Val453Ala
NM_017617.3:c.1358T>C	NP_060087.3:p.Val453Ala
XM_011518717.1:c.659T>C	XP_011517019.1:p.Val220Ala
NM_017617.5:c.1358T>C MANE Select	NP_060087.3:p.Val453Ala
XM_011518717.2:c.635T>C	XP_011517019.2:p.Val212Ala