Canonical Allele Identifier: CA467741901

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1251609154
• MyVariant Identifiers: chr9:g.139399127G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504675G>C , CM000671.2:g.136504675G>C	GRCh38
NC_000009.11:g.139399127G>C , CM000671.1:g.139399127G>C	GRCh37
NC_000009.10:g.138518948G>C	NCBI36
NG_007458.1:g.46112C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2823C>G
ENST00000651671.1:c.5016C>G MANE Select	ENSP00000498587.1:p.Arg1672=
ENST00000679595.1:c.5016C>G	ENSP00000506241.1:p.Arg1672=
ENST00000680133.1:c.4902C>G	ENSP00000505319.1:p.Arg1634=
ENST00000680218.1:c.4896C>G	ENSP00000505339.1:p.Arg1632=
ENST00000680668.1:c.4902C>G	ENSP00000506336.1:p.Arg1634=
ENST00000680778.1:c.2613C>G	ENSP00000506033.1:p.Arg871=
ENST00000680924.1:c.*2416C>G	ENSP00000506031.1:n.*2416C>G
ENST00000681135.1:c.*2625C>G	ENSP00000506636.1:n.*2625C>G
ENST00000681298.1:n.1829C>G
ENST00000681454.1:c.*4252C>G	ENSP00000505763.1:n.*4252C>G
ENST00000277541.6:c.5016C>G	ENSP00000277541.6:p.Arg1672=
ENST00000494783.1:n.171C>G
NM_017617.3:c.5016C>G	NP_060087.3:p.Arg1672=
XM_011518717.1:c.4317C>G	XP_011517019.1:p.Arg1439=
NM_017617.5:c.5016C>G MANE Select	NP_060087.3:p.Arg1672=
XM_011518717.2:c.4293C>G	XP_011517019.2:p.Arg1431=