Canonical Allele Identifier: CA467832522

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391750G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497298G>C , CM000671.2:g.136497298G>C	GRCh38
NC_000009.11:g.139391750G>C , CM000671.1:g.139391750G>C	GRCh37
NC_000009.10:g.138511571G>C	NCBI36
NG_007458.1:g.53489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6441C>G MANE Select	ENSP00000498587.1:p.Gly2147=
ENST00000679595.1:c.*1481C>G	ENSP00000506241.1:n.*1481C>G
ENST00000679969.1:n.3037C>G
ENST00000680003.1:n.2773C>G
ENST00000680133.1:c.6327C>G	ENSP00000505319.1:p.Gly2109=
ENST00000680218.1:c.6321C>G	ENSP00000505339.1:p.Gly2107=
ENST00000680668.1:c.6327C>G	ENSP00000506336.1:p.Gly2109=
ENST00000680778.1:c.4038C>G	ENSP00000506033.1:p.Gly1346=
ENST00000680924.1:c.*3841C>G	ENSP00000506031.1:n.*3841C>G
ENST00000681135.1:c.*4050C>G	ENSP00000506636.1:n.*4050C>G
ENST00000681298.1:n.4546C>G
ENST00000681454.1:c.*5677C>G	ENSP00000505763.1:n.*5677C>G
ENST00000277541.6:c.6441C>G	ENSP00000277541.6:p.Gly2147=
NM_017617.3:c.6441C>G	NP_060087.3:p.Gly2147=
XM_011518717.1:c.5742C>G	XP_011517019.1:p.Gly1914=
NM_017617.5:c.6441C>G MANE Select	NP_060087.3:p.Gly2147=
XM_011518717.2:c.5718C>G	XP_011517019.2:p.Gly1906=