Canonical Allele Identifier: CA375631250

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1346987070
• MyVariant Identifiers: chr9:g.139391629C>A (hg19) ; chr9:g.136497177C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497177C>A , CM000671.2:g.136497177C>A	GRCh38
NC_000009.11:g.139391629C>A , CM000671.1:g.139391629C>A	GRCh37
NC_000009.10:g.138511450C>A	NCBI36
NG_007458.1:g.53610G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6562G>T MANE Select	ENSP00000498587.1:p.Gly2188Cys
ENST00000679595.1:c.*1602G>T	ENSP00000506241.1:n.*1602G>T
ENST00000679969.1:n.3158G>T
ENST00000680003.1:n.2894G>T
ENST00000680133.1:c.6448G>T	ENSP00000505319.1:p.Gly2150Cys
ENST00000680218.1:c.6442G>T	ENSP00000505339.1:p.Gly2148Cys
ENST00000680668.1:c.6448G>T	ENSP00000506336.1:p.Gly2150Cys
ENST00000680778.1:c.4159G>T	ENSP00000506033.1:p.Gly1387Cys
ENST00000680924.1:c.*3962G>T	ENSP00000506031.1:n.*3962G>T
ENST00000681135.1:c.*4171G>T	ENSP00000506636.1:n.*4171G>T
ENST00000681298.1:n.4667G>T
ENST00000681454.1:c.*5798G>T	ENSP00000505763.1:n.*5798G>T
ENST00000277541.6:c.6562G>T	ENSP00000277541.6:p.Gly2188Cys
NM_017617.3:c.6562G>T	NP_060087.3:p.Gly2188Cys
XM_011518717.1:c.5863G>T	XP_011517019.1:p.Gly1955Cys
NM_017617.5:c.6562G>T MANE Select	NP_060087.3:p.Gly2188Cys
XM_011518717.2:c.5839G>T	XP_011517019.2:p.Gly1947Cys