Canonical Allele Identifier: CA375644220

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1381525257
• MyVariant Identifiers: chr9:g.139399182G>C (hg19) ; chr9:g.136504730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504730G>C , CM000671.2:g.136504730G>C	GRCh38
NC_000009.11:g.139399182G>C , CM000671.1:g.139399182G>C	GRCh37
NC_000009.10:g.138519003G>C	NCBI36
NG_007458.1:g.46057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2768C>G
ENST00000651671.1:c.4961C>G MANE Select	ENSP00000498587.1:p.Pro1654Arg
ENST00000679595.1:c.4961C>G	ENSP00000506241.1:p.Pro1654Arg
ENST00000680133.1:c.4847C>G	ENSP00000505319.1:p.Pro1616Arg
ENST00000680218.1:c.4841C>G	ENSP00000505339.1:p.Pro1614Arg
ENST00000680668.1:c.4847C>G	ENSP00000506336.1:p.Pro1616Arg
ENST00000680778.1:c.2558C>G	ENSP00000506033.1:p.Pro853Arg
ENST00000680924.1:c.*2361C>G	ENSP00000506031.1:n.*2361C>G
ENST00000681135.1:c.*2570C>G	ENSP00000506636.1:n.*2570C>G
ENST00000681298.1:n.1774C>G
ENST00000681454.1:c.*4197C>G	ENSP00000505763.1:n.*4197C>G
ENST00000277541.6:c.4961C>G	ENSP00000277541.6:p.Pro1654Arg
ENST00000494783.1:n.116C>G
NM_017617.3:c.4961C>G	NP_060087.3:p.Pro1654Arg
XM_011518717.1:c.4262C>G	XP_011517019.1:p.Pro1421Arg
NM_017617.5:c.4961C>G MANE Select	NP_060087.3:p.Pro1654Arg
XM_011518717.2:c.4238C>G	XP_011517019.2:p.Pro1413Arg