Canonical Allele Identifier: CA1884231181

Gene: NOTCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497184G= , CM000671.2:g.136497184G=	GRCh38
NC_000009.11:g.139391636G= , CM000671.1:g.139391636G=	GRCh37
NC_000009.10:g.138511457G=	NCBI36
NG_007458.1:g.53603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6555C= MANE Select	ENSP00000498587.1:p.Asp2185=
ENST00000679595.1:c.*1595C=	ENSP00000506241.1:n.*1595C=
ENST00000679969.1:n.3151C=
ENST00000680003.1:n.2887C=
ENST00000680133.1:c.6441C=	ENSP00000505319.1:p.Asp2147=
ENST00000680218.1:c.6435C=	ENSP00000505339.1:p.Asp2145=
ENST00000680668.1:c.6441C=	ENSP00000506336.1:p.Asp2147=
ENST00000680778.1:c.4152C=	ENSP00000506033.1:p.Asp1384=
ENST00000680924.1:c.*3955C=	ENSP00000506031.1:n.*3955C=
ENST00000681135.1:c.*4164C=	ENSP00000506636.1:n.*4164C=
ENST00000681298.1:n.4660C=
ENST00000681454.1:c.*5791C=	ENSP00000505763.1:n.*5791C=
ENST00000277541.6:c.6555C=	ENSP00000277541.6:p.Asp2185=
NM_017617.3:c.6555C=	NP_060087.3:p.Asp2185=
XM_011518717.1:c.5856C=	XP_011517019.1:p.Asp1952=
NM_017617.5:c.6555C= MANE Select	NP_060087.3:p.Asp2185=
XM_011518717.2:c.5832C=	XP_011517019.2:p.Asp1944=