Canonical Allele Identifier: CA375631167

Gene: NOTCH1

Linked Data

• dbSNP Id: rs755029006
• gnomAD v4: 9-136497155-C-T
• MyVariant Identifiers: chr9:g.139391607C>T (hg19) ; chr9:g.136497155C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497155C>T , CM000671.2:g.136497155C>T	GRCh38
NC_000009.11:g.139391607C>T , CM000671.1:g.139391607C>T	GRCh37
NC_000009.10:g.138511428C>T	NCBI36
NG_007458.1:g.53632G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6584G>A MANE Select	ENSP00000498587.1:p.Gly2195Asp
ENST00000679595.1:c.*1624G>A	ENSP00000506241.1:n.*1624G>A
ENST00000679969.1:n.3180G>A
ENST00000680003.1:n.2916G>A
ENST00000680133.1:c.6470G>A	ENSP00000505319.1:p.Gly2157Asp
ENST00000680218.1:c.6464G>A	ENSP00000505339.1:p.Gly2155Asp
ENST00000680668.1:c.6470G>A	ENSP00000506336.1:p.Gly2157Asp
ENST00000680778.1:c.4181G>A	ENSP00000506033.1:p.Gly1394Asp
ENST00000680924.1:c.*3984G>A	ENSP00000506031.1:n.*3984G>A
ENST00000681135.1:c.*4193G>A	ENSP00000506636.1:n.*4193G>A
ENST00000681298.1:n.4689G>A
ENST00000681454.1:c.*5820G>A	ENSP00000505763.1:n.*5820G>A
ENST00000277541.6:c.6584G>A	ENSP00000277541.6:p.Gly2195Asp
NM_017617.3:c.6584G>A	NP_060087.3:p.Gly2195Asp
XM_011518717.1:c.5885G>A	XP_011517019.1:p.Gly1962Asp
NM_017617.5:c.6584G>A MANE Select	NP_060087.3:p.Gly2195Asp
XM_011518717.2:c.5861G>A	XP_011517019.2:p.Gly1954Asp