Canonical Allele Identifier: CA467741928

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136504710-G-T
• MyVariant Identifiers: chr9:g.139399162G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504710G>T , CM000671.2:g.136504710G>T	GRCh38
NC_000009.11:g.139399162G>T , CM000671.1:g.139399162G>T	GRCh37
NC_000009.10:g.138518983G>T	NCBI36
NG_007458.1:g.46077C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2788C>A
ENST00000651671.1:c.4981C>A MANE Select	ENSP00000498587.1:p.Arg1661=
ENST00000679595.1:c.4981C>A	ENSP00000506241.1:p.Arg1661=
ENST00000680133.1:c.4867C>A	ENSP00000505319.1:p.Arg1623=
ENST00000680218.1:c.4861C>A	ENSP00000505339.1:p.Arg1621=
ENST00000680668.1:c.4867C>A	ENSP00000506336.1:p.Arg1623=
ENST00000680778.1:c.2578C>A	ENSP00000506033.1:p.Arg860=
ENST00000680924.1:c.*2381C>A	ENSP00000506031.1:n.*2381C>A
ENST00000681135.1:c.*2590C>A	ENSP00000506636.1:n.*2590C>A
ENST00000681298.1:n.1794C>A
ENST00000681454.1:c.*4217C>A	ENSP00000505763.1:n.*4217C>A
ENST00000277541.6:c.4981C>A	ENSP00000277541.6:p.Arg1661=
ENST00000494783.1:n.136C>A
NM_017617.3:c.4981C>A	NP_060087.3:p.Arg1661=
XM_011518717.1:c.4282C>A	XP_011517019.1:p.Arg1428=
NM_017617.5:c.4981C>A MANE Select	NP_060087.3:p.Arg1661=
XM_011518717.2:c.4258C>A	XP_011517019.2:p.Arg1420=