Canonical Allele Identifier: CA375644292

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136504746-T-C
• MyVariant Identifiers: chr9:g.139399198T>C (hg19) ; chr9:g.136504746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504746T>C , CM000671.2:g.136504746T>C	GRCh38
NC_000009.11:g.139399198T>C , CM000671.1:g.139399198T>C	GRCh37
NC_000009.10:g.138519019T>C	NCBI36
NG_007458.1:g.46041A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2752A>G
ENST00000651671.1:c.4945A>G MANE Select	ENSP00000498587.1:p.Lys1649Glu
ENST00000679595.1:c.4945A>G	ENSP00000506241.1:p.Lys1649Glu
ENST00000680133.1:c.4831A>G	ENSP00000505319.1:p.Lys1611Glu
ENST00000680218.1:c.4825A>G	ENSP00000505339.1:p.Lys1609Glu
ENST00000680668.1:c.4831A>G	ENSP00000506336.1:p.Lys1611Glu
ENST00000680778.1:c.2542A>G	ENSP00000506033.1:p.Lys848Glu
ENST00000680924.1:c.*2345A>G	ENSP00000506031.1:n.*2345A>G
ENST00000681135.1:c.*2554A>G	ENSP00000506636.1:n.*2554A>G
ENST00000681298.1:n.1758A>G
ENST00000681454.1:c.*4181A>G	ENSP00000505763.1:n.*4181A>G
ENST00000277541.6:c.4945A>G	ENSP00000277541.6:p.Lys1649Glu
ENST00000494783.1:n.100A>G
NM_017617.3:c.4945A>G	NP_060087.3:p.Lys1649Glu
XM_011518717.1:c.4246A>G	XP_011517019.1:p.Lys1416Glu
NM_017617.5:c.4945A>G MANE Select	NP_060087.3:p.Lys1649Glu
XM_011518717.2:c.4222A>G	XP_011517019.2:p.Lys1408Glu