Canonical Allele Identifier: CA375631415

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1203783810
• MyVariant Identifiers: chr9:g.139391669C>A (hg19) ; chr9:g.136497217C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497217C>A , CM000671.2:g.136497217C>A	GRCh38
NC_000009.11:g.139391669C>A , CM000671.1:g.139391669C>A	GRCh37
NC_000009.10:g.138511490C>A	NCBI36
NG_007458.1:g.53570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6522G>T MANE Select	ENSP00000498587.1:p.Lys2174Asn
ENST00000679595.1:c.*1562G>T	ENSP00000506241.1:n.*1562G>T
ENST00000679969.1:n.3118G>T
ENST00000680003.1:n.2854G>T
ENST00000680133.1:c.6408G>T	ENSP00000505319.1:p.Lys2136Asn
ENST00000680218.1:c.6402G>T	ENSP00000505339.1:p.Lys2134Asn
ENST00000680668.1:c.6408G>T	ENSP00000506336.1:p.Lys2136Asn
ENST00000680778.1:c.4119G>T	ENSP00000506033.1:p.Lys1373Asn
ENST00000680924.1:c.*3922G>T	ENSP00000506031.1:n.*3922G>T
ENST00000681135.1:c.*4131G>T	ENSP00000506636.1:n.*4131G>T
ENST00000681298.1:n.4627G>T
ENST00000681454.1:c.*5758G>T	ENSP00000505763.1:n.*5758G>T
ENST00000277541.6:c.6522G>T	ENSP00000277541.6:p.Lys2174Asn
NM_017617.3:c.6522G>T	NP_060087.3:p.Lys2174Asn
XM_011518717.1:c.5823G>T	XP_011517019.1:p.Lys1941Asn
NM_017617.5:c.6522G>T MANE Select	NP_060087.3:p.Lys2174Asn
XM_011518717.2:c.5799G>T	XP_011517019.2:p.Lys1933Asn