Canonical Allele Identifier: CA375634204

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1589054520
• MyVariant Identifiers: chr9:g.139393562A>C (hg19) ; chr9:g.136499110A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136499110A>C , CM000671.2:g.136499110A>C	GRCh38
NC_000009.11:g.139393562A>C , CM000671.1:g.139393562A>C	GRCh37
NC_000009.10:g.138513383A>C	NCBI36
NG_007458.1:g.51677T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6082+2T>G MANE Select	ENSP00000498587.1:n.6082+2T>G
ENST00000679595.1:c.*1122+2T>G	ENSP00000506241.1:n.*1122+2T>G
ENST00000679969.1:n.2565T>G
ENST00000680003.1:n.2414+2T>G
ENST00000680133.1:c.5968+2T>G	ENSP00000505319.1:n.5968+2T>G
ENST00000680218.1:c.5962+2T>G	ENSP00000505339.1:n.5962+2T>G
ENST00000680668.1:c.5968+2T>G	ENSP00000506336.1:n.5968+2T>G
ENST00000680778.1:c.3679+2T>G	ENSP00000506033.1:n.3679+2T>G
ENST00000680924.1:c.*3482+2T>G	ENSP00000506031.1:n.*3482+2T>G
ENST00000681135.1:c.*3691+2T>G	ENSP00000506636.1:n.*3691+2T>G
ENST00000681298.1:n.4187+2T>G
ENST00000681454.1:c.*5318+2T>G	ENSP00000505763.1:n.*5318+2T>G
ENST00000277541.6:c.6082+2T>G	ENSP00000277541.6:n.6082+2T>G
NM_017617.3:c.6082+2T>G	NP_060087.3:n.6082+2T>G
XM_011518717.1:c.5383+2T>G	XP_011517019.1:n.5383+2T>G
NM_017617.5:c.6082+2T>G MANE Select	NP_060087.3:n.6082+2T>G
XM_011518717.2:c.5359+2T>G	XP_011517019.2:n.5359+2T>G