Canonical Allele Identifier: CA375631390

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391664A>C (hg19) ; chr9:g.136497212A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497212A>C , CM000671.2:g.136497212A>C	GRCh38
NC_000009.11:g.139391664A>C , CM000671.1:g.139391664A>C	GRCh37
NC_000009.10:g.138511485A>C	NCBI36
NG_007458.1:g.53575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6527T>G MANE Select	ENSP00000498587.1:p.Leu2176Arg
ENST00000679595.1:c.*1567T>G	ENSP00000506241.1:n.*1567T>G
ENST00000679969.1:n.3123T>G
ENST00000680003.1:n.2859T>G
ENST00000680133.1:c.6413T>G	ENSP00000505319.1:p.Leu2138Arg
ENST00000680218.1:c.6407T>G	ENSP00000505339.1:p.Leu2136Arg
ENST00000680668.1:c.6413T>G	ENSP00000506336.1:p.Leu2138Arg
ENST00000680778.1:c.4124T>G	ENSP00000506033.1:p.Leu1375Arg
ENST00000680924.1:c.*3927T>G	ENSP00000506031.1:n.*3927T>G
ENST00000681135.1:c.*4136T>G	ENSP00000506636.1:n.*4136T>G
ENST00000681298.1:n.4632T>G
ENST00000681454.1:c.*5763T>G	ENSP00000505763.1:n.*5763T>G
ENST00000277541.6:c.6527T>G	ENSP00000277541.6:p.Leu2176Arg
NM_017617.3:c.6527T>G	NP_060087.3:p.Leu2176Arg
XM_011518717.1:c.5828T>G	XP_011517019.1:p.Leu1943Arg
NM_017617.5:c.6527T>G MANE Select	NP_060087.3:p.Leu2176Arg
XM_011518717.2:c.5804T>G	XP_011517019.2:p.Leu1935Arg