Canonical Allele Identifier: CA375643901

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1226514285
• gnomAD v4: 9-136504674-C-G
• MyVariant Identifiers: chr9:g.139399126C>G (hg19) ; chr9:g.136504674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504674C>G , CM000671.2:g.136504674C>G	GRCh38
NC_000009.11:g.139399126C>G , CM000671.1:g.139399126C>G	GRCh37
NC_000009.10:g.138518947C>G	NCBI36
NG_007458.1:g.46113G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2824G>C
ENST00000651671.1:c.5017G>C MANE Select	ENSP00000498587.1:p.Gly1673Arg
ENST00000679595.1:c.5017G>C	ENSP00000506241.1:p.Gly1673Arg
ENST00000680133.1:c.4903G>C	ENSP00000505319.1:p.Gly1635Arg
ENST00000680218.1:c.4897G>C	ENSP00000505339.1:p.Gly1633Arg
ENST00000680668.1:c.4903G>C	ENSP00000506336.1:p.Gly1635Arg
ENST00000680778.1:c.2614G>C	ENSP00000506033.1:p.Gly872Arg
ENST00000680924.1:c.*2417G>C	ENSP00000506031.1:n.*2417G>C
ENST00000681135.1:c.*2626G>C	ENSP00000506636.1:n.*2626G>C
ENST00000681298.1:n.1830G>C
ENST00000681454.1:c.*4253G>C	ENSP00000505763.1:n.*4253G>C
ENST00000277541.6:c.5017G>C	ENSP00000277541.6:p.Gly1673Arg
ENST00000494783.1:n.172G>C
NM_017617.3:c.5017G>C	NP_060087.3:p.Gly1673Arg
XM_011518717.1:c.4318G>C	XP_011517019.1:p.Gly1440Arg
NM_017617.5:c.5017G>C MANE Select	NP_060087.3:p.Gly1673Arg
XM_011518717.2:c.4294G>C	XP_011517019.2:p.Gly1432Arg