Canonical Allele Identifier: CA2832602851

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504882G= , CM000671.2:g.136504882G=	GRCh38
NC_000009.11:g.139399334G= , CM000671.1:g.139399334G=	GRCh37
NC_000009.10:g.138519155G=	NCBI36
NG_007458.1:g.45905C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2616C=
ENST00000651671.1:c.4809C= MANE Select	ENSP00000498587.1:p.Asn1603=
ENST00000679595.1:c.4809C=	ENSP00000506241.1:p.Asn1603=
ENST00000680133.1:c.4695C=	ENSP00000505319.1:p.Asn1565=
ENST00000680218.1:c.4689C=	ENSP00000505339.1:p.Asn1563=
ENST00000680668.1:c.4695C=	ENSP00000506336.1:p.Asn1565=
ENST00000680778.1:c.2406C=	ENSP00000506033.1:p.Asn802=
ENST00000680924.1:c.*2209C=	ENSP00000506031.1:n.*2209C=
ENST00000681135.1:c.*2418C=	ENSP00000506636.1:n.*2418C=
ENST00000681298.1:n.1622C=
ENST00000681454.1:c.*4045C=	ENSP00000505763.1:n.*4045C=
ENST00000277541.6:c.4809C=	ENSP00000277541.6:p.Asn1603=
NM_017617.3:c.4809C=	NP_060087.3:p.Asn1603=
XM_011518717.1:c.4110C=	XP_011517019.1:p.Asn1370=
NM_017617.5:c.4809C= MANE Select	NP_060087.3:p.Asn1603=
XM_011518717.2:c.4086C=	XP_011517019.2:p.Asn1362=