Canonical Allele Identifier: CA1884231214

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497222C= , CM000671.2:g.136497222C=	GRCh38
NC_000009.11:g.139391674C= , CM000671.1:g.139391674C=	GRCh37
NC_000009.10:g.138511495C=	NCBI36
NG_007458.1:g.53565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6517G= MANE Select	ENSP00000498587.1:p.Ala2173=
ENST00000679595.1:c.*1557G=	ENSP00000506241.1:n.*1557G=
ENST00000679969.1:n.3113G=
ENST00000680003.1:n.2849G=
ENST00000680133.1:c.6403G=	ENSP00000505319.1:p.Ala2135=
ENST00000680218.1:c.6397G=	ENSP00000505339.1:p.Ala2133=
ENST00000680668.1:c.6403G=	ENSP00000506336.1:p.Ala2135=
ENST00000680778.1:c.4114G=	ENSP00000506033.1:p.Ala1372=
ENST00000680924.1:c.*3917G=	ENSP00000506031.1:n.*3917G=
ENST00000681135.1:c.*4126G=	ENSP00000506636.1:n.*4126G=
ENST00000681298.1:n.4622G=
ENST00000681454.1:c.*5753G=	ENSP00000505763.1:n.*5753G=
ENST00000277541.6:c.6517G=	ENSP00000277541.6:p.Ala2173=
NM_017617.3:c.6517G=	NP_060087.3:p.Ala2173=
XM_011518717.1:c.5818G=	XP_011517019.1:p.Ala1940=
NM_017617.5:c.6517G= MANE Select	NP_060087.3:p.Ala2173=
XM_011518717.2:c.5794G=	XP_011517019.2:p.Ala1932=