Canonical Allele Identifier: CA2692633453

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136498828-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498828G>T , CM000671.2:g.136498828G>T	GRCh38
NC_000009.11:g.139393280G>T , CM000671.1:g.139393280G>T	GRCh37
NC_000009.10:g.138513101G>T	NCBI36
NG_007458.1:g.51959C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000651671.1:c.6180+71C>A MANE Select	ENSP00000498587.1:n.6180+71C>A
ENST00000679595.1:c.*1220+71C>A	ENSP00000506241.1:n.*1220+71C>A
ENST00000679969.1:n.2776+71C>A
ENST00000680003.1:n.2512+71C>A
ENST00000680133.1:c.6066+71C>A	ENSP00000505319.1:n.6066+71C>A
ENST00000680218.1:c.6060+71C>A	ENSP00000505339.1:n.6060+71C>A
ENST00000680668.1:c.6066+71C>A	ENSP00000506336.1:n.6066+71C>A
ENST00000680778.1:c.3777+71C>A	ENSP00000506033.1:n.3777+71C>A
ENST00000680924.1:c.*3580+71C>A	ENSP00000506031.1:n.*3580+71C>A
ENST00000681135.1:c.*3789+71C>A	ENSP00000506636.1:n.*3789+71C>A
ENST00000681298.1:n.4285+71C>A
ENST00000681454.1:c.*5416+71C>A	ENSP00000505763.1:n.*5416+71C>A
ENST00000277541.6:c.6180+71C>A	ENSP00000277541.6:n.6180+71C>A
NM_017617.3:c.6180+71C>A	NP_060087.3:n.6180+71C>A
XM_011518717.1:c.5481+71C>A	XP_011517019.1:n.5481+71C>A
NM_017617.5:c.6180+71C>A MANE Select	NP_060087.3:n.6180+71C>A
XM_011518717.2:c.5457+71C>A	XP_011517019.2:n.5457+71C>A