Canonical Allele Identifier: CA375562893

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1843299996
• MyVariant Identifiers: chr9:g.139412230C>G (hg19) ; chr9:g.136517778C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136517778C>G , CM000671.2:g.136517778C>G	GRCh38
NC_000009.11:g.139412230C>G , CM000671.1:g.139412230C>G	GRCh37
NC_000009.10:g.138532051C>G	NCBI36
NG_007458.1:g.33009G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.1415G>C MANE Select	ENSP00000498587.1:p.Gly472Ala
ENST00000679595.1:c.1415G>C	ENSP00000506241.1:p.Gly472Ala
ENST00000680133.1:c.1415G>C	ENSP00000505319.1:p.Gly472Ala
ENST00000680218.1:c.1415G>C	ENSP00000505339.1:p.Gly472Ala
ENST00000680668.1:c.1415G>C	ENSP00000506336.1:p.Gly472Ala
ENST00000680924.1:c.1415G>C	ENSP00000506031.1:p.Gly472Ala
ENST00000681135.1:c.1415G>C	ENSP00000506636.1:p.Gly472Ala
ENST00000681454.1:c.*651G>C	ENSP00000505763.1:n.*651G>C
ENST00000277541.6:c.1415G>C	ENSP00000277541.6:p.Gly472Ala
NM_017617.3:c.1415G>C	NP_060087.3:p.Gly472Ala
XM_011518717.1:c.716G>C	XP_011517019.1:p.Gly239Ala
NM_017617.5:c.1415G>C MANE Select	NP_060087.3:p.Gly472Ala
XM_011518717.2:c.692G>C	XP_011517019.2:p.Gly231Ala