Canonical Allele Identifier: CA467741917

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136504702-C-A
• MyVariant Identifiers: chr9:g.139399154C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504702C>A , CM000671.2:g.136504702C>A	GRCh38
NC_000009.11:g.139399154C>A , CM000671.1:g.139399154C>A	GRCh37
NC_000009.10:g.138518975C>A	NCBI36
NG_007458.1:g.46085G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2796G>T
ENST00000651671.1:c.4989G>T MANE Select	ENSP00000498587.1:p.Arg1663=
ENST00000679595.1:c.4989G>T	ENSP00000506241.1:p.Arg1663=
ENST00000680133.1:c.4875G>T	ENSP00000505319.1:p.Arg1625=
ENST00000680218.1:c.4869G>T	ENSP00000505339.1:p.Arg1623=
ENST00000680668.1:c.4875G>T	ENSP00000506336.1:p.Arg1625=
ENST00000680778.1:c.2586G>T	ENSP00000506033.1:p.Arg862=
ENST00000680924.1:c.*2389G>T	ENSP00000506031.1:n.*2389G>T
ENST00000681135.1:c.*2598G>T	ENSP00000506636.1:n.*2598G>T
ENST00000681298.1:n.1802G>T
ENST00000681454.1:c.*4225G>T	ENSP00000505763.1:n.*4225G>T
ENST00000277541.6:c.4989G>T	ENSP00000277541.6:p.Arg1663=
ENST00000494783.1:n.144G>T
NM_017617.3:c.4989G>T	NP_060087.3:p.Arg1663=
XM_011518717.1:c.4290G>T	XP_011517019.1:p.Arg1430=
NM_017617.5:c.4989G>T MANE Select	NP_060087.3:p.Arg1663=
XM_011518717.2:c.4266G>T	XP_011517019.2:p.Arg1422=