Canonical Allele Identifier: CA201587586

Gene: NOTCH1

Linked Data

• dbSNP Id: rs34963797
• MyVariant Identifiers: chr9:g.139412475_139412476insG (hg19) ; chr9:g.136518023_136518024insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136518026dup , CM000671.2:g.136518026dup	GRCh38
NC_000009.11:g.139412478dup , CM000671.1:g.139412478dup	GRCh37
NC_000009.10:g.138532299dup	NCBI36
NG_007458.1:g.32763dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.1256-87dup MANE Select	ENSP00000498587.1:n.1256-87dup
ENST00000679595.1:c.1256-87dup	ENSP00000506241.1:n.1256-87dup
ENST00000680133.1:c.1256-87dup	ENSP00000505319.1:n.1256-87dup
ENST00000680218.1:c.1256-87dup	ENSP00000505339.1:n.1256-87dup
ENST00000680668.1:c.1256-87dup	ENSP00000506336.1:n.1256-87dup
ENST00000680924.1:c.1256-87dup	ENSP00000506031.1:n.1256-87dup
ENST00000681135.1:c.1256-87dup	ENSP00000506636.1:n.1256-87dup
ENST00000681454.1:c.*492-87dup	ENSP00000505763.1:n.*492-87dup
ENST00000277541.6:c.1256-87dup	ENSP00000277541.6:n.1256-87dup
NM_017617.3:c.1256-87dup	NP_060087.3:n.1256-87dup
XM_011518717.1:c.557-87dup	XP_011517019.1:n.557-87dup
NM_017617.5:c.1256-87dup MANE Select	NP_060087.3:n.1256-87dup
XM_011518717.2:c.533-87dup	XP_011517019.2:n.533-87dup