Canonical Allele Identifier: CA375644290

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139399198T>A (hg19) ; chr9:g.136504746T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2752A>T
ENST00000651671.1:c.4945A>T MANE Select	ENSP00000498587.1:p.Lys1649Ter
ENST00000679595.1:c.4945A>T	ENSP00000506241.1:p.Lys1649Ter
ENST00000680133.1:c.4831A>T	ENSP00000505319.1:p.Lys1611Ter
ENST00000680218.1:c.4825A>T	ENSP00000505339.1:p.Lys1609Ter
ENST00000680668.1:c.4831A>T	ENSP00000506336.1:p.Lys1611Ter
ENST00000680778.1:c.2542A>T	ENSP00000506033.1:p.Lys848Ter
ENST00000680924.1:c.*2345A>T	ENSP00000506031.1:n.*2345A>T
ENST00000681135.1:c.*2554A>T	ENSP00000506636.1:n.*2554A>T
ENST00000681298.1:n.1758A>T
ENST00000681454.1:c.*4181A>T	ENSP00000505763.1:n.*4181A>T
ENST00000277541.6:c.4945A>T	ENSP00000277541.6:p.Lys1649Ter
ENST00000494783.1:n.100A>T
NM_017617.3:c.4945A>T	NP_060087.3:p.Lys1649Ter
XM_011518717.1:c.4246A>T	XP_011517019.1:p.Lys1416Ter
NM_017617.5:c.4945A>T MANE Select	NP_060087.3:p.Lys1649Ter
XM_011518717.2:c.4222A>T	XP_011517019.2:p.Lys1408Ter