Canonical Allele Identifier: CA375631843

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391796G>T (hg19) ; chr9:g.136497344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497344G>T , CM000671.2:g.136497344G>T	GRCh38
NC_000009.11:g.139391796G>T , CM000671.1:g.139391796G>T	GRCh37
NC_000009.10:g.138511617G>T	NCBI36
NG_007458.1:g.53443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6395C>A MANE Select	ENSP00000498587.1:p.Thr2132Lys
ENST00000679595.1:c.*1435C>A	ENSP00000506241.1:n.*1435C>A
ENST00000679969.1:n.2991C>A
ENST00000680003.1:n.2727C>A
ENST00000680133.1:c.6281C>A	ENSP00000505319.1:p.Thr2094Lys
ENST00000680218.1:c.6275C>A	ENSP00000505339.1:p.Thr2092Lys
ENST00000680668.1:c.6281C>A	ENSP00000506336.1:p.Thr2094Lys
ENST00000680778.1:c.3992C>A	ENSP00000506033.1:p.Thr1331Lys
ENST00000680924.1:c.*3795C>A	ENSP00000506031.1:n.*3795C>A
ENST00000681135.1:c.*4004C>A	ENSP00000506636.1:n.*4004C>A
ENST00000681298.1:n.4500C>A
ENST00000681454.1:c.*5631C>A	ENSP00000505763.1:n.*5631C>A
ENST00000277541.6:c.6395C>A	ENSP00000277541.6:p.Thr2132Lys
NM_017617.3:c.6395C>A	NP_060087.3:p.Thr2132Lys
XM_011518717.1:c.5696C>A	XP_011517019.1:p.Thr1899Lys
NM_017617.5:c.6395C>A MANE Select	NP_060087.3:p.Thr2132Lys
XM_011518717.2:c.5672C>A	XP_011517019.2:p.Thr1891Lys