Canonical Allele Identifier: CA1884232351

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498813G= , CM000671.2:g.136498813G=	GRCh38
NC_000009.11:g.139393265G= , CM000671.1:g.139393265G=	GRCh37
NC_000009.10:g.138513086G=	NCBI36
NG_007458.1:g.51974C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000651671.1:c.6180+86C= MANE Select	ENSP00000498587.1:n.6180+86C=
ENST00000679595.1:c.*1220+86C=	ENSP00000506241.1:n.*1220+86C=
ENST00000679969.1:n.2776+86C=
ENST00000680003.1:n.2512+86C=
ENST00000680133.1:c.6066+86C=	ENSP00000505319.1:n.6066+86C=
ENST00000680218.1:c.6060+86C=	ENSP00000505339.1:n.6060+86C=
ENST00000680668.1:c.6066+86C=	ENSP00000506336.1:n.6066+86C=
ENST00000680778.1:c.3777+86C=	ENSP00000506033.1:n.3777+86C=
ENST00000680924.1:c.*3580+86C=	ENSP00000506031.1:n.*3580+86C=
ENST00000681135.1:c.*3789+86C=	ENSP00000506636.1:n.*3789+86C=
ENST00000681298.1:n.4285+86C=
ENST00000681454.1:c.*5416+86C=	ENSP00000505763.1:n.*5416+86C=
ENST00000277541.6:c.6180+86C=	ENSP00000277541.6:n.6180+86C=
NM_017617.3:c.6180+86C=	NP_060087.3:n.6180+86C=
XM_011518717.1:c.5481+86C=	XP_011517019.1:n.5481+86C=
NM_017617.5:c.6180+86C= MANE Select	NP_060087.3:n.6180+86C=
XM_011518717.2:c.5457+86C=	XP_011517019.2:n.5457+86C=