Canonical Allele Identifier: CA375644155

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133335815
• gnomAD v4: 9-136504715-C-G
• MyVariant Identifiers: chr9:g.139399167C>G (hg19) ; chr9:g.136504715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504715C>G , CM000671.2:g.136504715C>G	GRCh38
NC_000009.11:g.139399167C>G , CM000671.1:g.139399167C>G	GRCh37
NC_000009.10:g.138518988C>G	NCBI36
NG_007458.1:g.46072G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2783G>C
ENST00000651671.1:c.4976G>C MANE Select	ENSP00000498587.1:p.Gly1659Ala
ENST00000679595.1:c.4976G>C	ENSP00000506241.1:p.Gly1659Ala
ENST00000680133.1:c.4862G>C	ENSP00000505319.1:p.Gly1621Ala
ENST00000680218.1:c.4856G>C	ENSP00000505339.1:p.Gly1619Ala
ENST00000680668.1:c.4862G>C	ENSP00000506336.1:p.Gly1621Ala
ENST00000680778.1:c.2573G>C	ENSP00000506033.1:p.Gly858Ala
ENST00000680924.1:c.*2376G>C	ENSP00000506031.1:n.*2376G>C
ENST00000681135.1:c.*2585G>C	ENSP00000506636.1:n.*2585G>C
ENST00000681298.1:n.1789G>C
ENST00000681454.1:c.*4212G>C	ENSP00000505763.1:n.*4212G>C
ENST00000277541.6:c.4976G>C	ENSP00000277541.6:p.Gly1659Ala
ENST00000494783.1:n.131G>C
NM_017617.3:c.4976G>C	NP_060087.3:p.Gly1659Ala
XM_011518717.1:c.4277G>C	XP_011517019.1:p.Gly1426Ala
NM_017617.5:c.4976G>C MANE Select	NP_060087.3:p.Gly1659Ala
XM_011518717.2:c.4253G>C	XP_011517019.2:p.Gly1418Ala