Canonical Allele Identifier: CA375644231

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133335894
• MyVariant Identifiers: chr9:g.139399185A>G (hg19) ; chr9:g.136504733A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504733A>G , CM000671.2:g.136504733A>G	GRCh38
NC_000009.11:g.139399185A>G , CM000671.1:g.139399185A>G	GRCh37
NC_000009.10:g.138519006A>G	NCBI36
NG_007458.1:g.46054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2765T>C
ENST00000651671.1:c.4958T>C MANE Select	ENSP00000498587.1:p.Leu1653Pro
ENST00000679595.1:c.4958T>C	ENSP00000506241.1:p.Leu1653Pro
ENST00000680133.1:c.4844T>C	ENSP00000505319.1:p.Leu1615Pro
ENST00000680218.1:c.4838T>C	ENSP00000505339.1:p.Leu1613Pro
ENST00000680668.1:c.4844T>C	ENSP00000506336.1:p.Leu1615Pro
ENST00000680778.1:c.2555T>C	ENSP00000506033.1:p.Leu852Pro
ENST00000680924.1:c.*2358T>C	ENSP00000506031.1:n.*2358T>C
ENST00000681135.1:c.*2567T>C	ENSP00000506636.1:n.*2567T>C
ENST00000681298.1:n.1771T>C
ENST00000681454.1:c.*4194T>C	ENSP00000505763.1:n.*4194T>C
ENST00000277541.6:c.4958T>C	ENSP00000277541.6:p.Leu1653Pro
ENST00000494783.1:n.113T>C
NM_017617.3:c.4958T>C	NP_060087.3:p.Leu1653Pro
XM_011518717.1:c.4259T>C	XP_011517019.1:p.Leu1420Pro
NM_017617.5:c.4958T>C MANE Select	NP_060087.3:p.Leu1653Pro
XM_011518717.2:c.4235T>C	XP_011517019.2:p.Leu1412Pro