Canonical Allele Identifier: CA2721107574

Gene: NOTCH1

Linked Data

• dbSNP Id: rs2133322305

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136499072C>T , CM000671.2:g.136499072C>T	GRCh38
NC_000009.11:g.139393524C>T , CM000671.1:g.139393524C>T	GRCh37
NC_000009.10:g.138513345C>T	NCBI36
NG_007458.1:g.51715G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6082+40G>A MANE Select	ENSP00000498587.1:n.6082+40G>A
ENST00000679595.1:c.*1122+40G>A	ENSP00000506241.1:n.*1122+40G>A
ENST00000679969.1:n.2603G>A
ENST00000680003.1:n.2414+40G>A
ENST00000680133.1:c.5968+40G>A	ENSP00000505319.1:n.5968+40G>A
ENST00000680218.1:c.5962+40G>A	ENSP00000505339.1:n.5962+40G>A
ENST00000680668.1:c.5968+40G>A	ENSP00000506336.1:n.5968+40G>A
ENST00000680778.1:c.3679+40G>A	ENSP00000506033.1:n.3679+40G>A
ENST00000680924.1:c.*3482+40G>A	ENSP00000506031.1:n.*3482+40G>A
ENST00000681135.1:c.*3691+40G>A	ENSP00000506636.1:n.*3691+40G>A
ENST00000681298.1:n.4187+40G>A
ENST00000681454.1:c.*5318+40G>A	ENSP00000505763.1:n.*5318+40G>A
ENST00000277541.6:c.6082+40G>A	ENSP00000277541.6:n.6082+40G>A
NM_017617.3:c.6082+40G>A	NP_060087.3:n.6082+40G>A
XM_011518717.1:c.5383+40G>A	XP_011517019.1:n.5383+40G>A
NM_017617.5:c.6082+40G>A MANE Select	NP_060087.3:n.6082+40G>A
XM_011518717.2:c.5359+40G>A	XP_011517019.2:n.5359+40G>A