Canonical Allele Identifier: CA12976372

Gene: NOTCH1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136531182A>G , CM000671.2:g.136531182A>G	GRCh38
NC_000009.11:g.139425634A>G , CM000671.1:g.139425634A>G	GRCh37
NC_000009.10:g.138545455A>G	NCBI36
NG_007458.1:g.19605T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.141-7203T>C MANE Select	ENSP00000498587.1:n.141-7203T>C
ENST00000679595.1:c.141-7203T>C	ENSP00000506241.1:n.141-7203T>C
ENST00000680133.1:c.141-7203T>C	ENSP00000505319.1:n.141-7203T>C
ENST00000680218.1:c.141-7203T>C	ENSP00000505339.1:n.141-7203T>C
ENST00000680668.1:c.141-7203T>C	ENSP00000506336.1:n.141-7203T>C
ENST00000680924.1:c.141-7203T>C	ENSP00000506031.1:n.141-7203T>C
ENST00000681135.1:c.141-7203T>C	ENSP00000506636.1:n.141-7203T>C
ENST00000681454.1:c.141-11617T>C	ENSP00000505763.1:n.141-11617T>C
ENST00000277541.6:c.141-7203T>C	ENSP00000277541.6:n.141-7203T>C
NM_017617.3:c.141-7203T>C	NP_060087.3:n.141-7203T>C
XM_011518717.1:c.44-11617T>C	XP_011517019.1:n.44-11617T>C
XR_930441.1:n.3450A>G
NM_017617.5:c.141-7203T>C MANE Select	NP_060087.3:n.141-7203T>C
XM_011518717.2:c.20-11617T>C	XP_011517019.2:n.20-11617T>C