Canonical Allele Identifier: CA2721108949

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133338002

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136505136T>G , CM000671.2:g.136505136T>G	GRCh38
NC_000009.11:g.139399588T>G , CM000671.1:g.139399588T>G	GRCh37
NC_000009.10:g.138519409T>G	NCBI36
NG_007458.1:g.45651A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2394-32A>C
ENST00000651671.1:c.4587-32A>C MANE Select	ENSP00000498587.1:n.4587-32A>C
ENST00000679595.1:c.4587-32A>C	ENSP00000506241.1:n.4587-32A>C
ENST00000680133.1:c.4473-32A>C	ENSP00000505319.1:n.4473-32A>C
ENST00000680218.1:c.4467-32A>C	ENSP00000505339.1:n.4467-32A>C
ENST00000680668.1:c.4473-32A>C	ENSP00000506336.1:n.4473-32A>C
ENST00000680778.1:c.2184-32A>C	ENSP00000506033.1:n.2184-32A>C
ENST00000680924.1:c.*1987-32A>C	ENSP00000506031.1:n.*1987-32A>C
ENST00000681135.1:c.*2196-32A>C	ENSP00000506636.1:n.*2196-32A>C
ENST00000681298.1:n.1400-32A>C
ENST00000681454.1:c.*3823-32A>C	ENSP00000505763.1:n.*3823-32A>C
ENST00000277541.6:c.4587-32A>C	ENSP00000277541.6:n.4587-32A>C
NM_017617.3:c.4587-32A>C	NP_060087.3:n.4587-32A>C
XM_011518717.1:c.3888-32A>C	XP_011517019.1:n.3888-32A>C
NM_017617.5:c.4587-32A>C MANE Select	NP_060087.3:n.4587-32A>C
XM_011518717.2:c.3864-32A>C	XP_011517019.2:n.3864-32A>C