Canonical Allele Identifier: CA375631866

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391809G>C (hg19) ; chr9:g.136497357G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497357G>C , CM000671.2:g.136497357G>C	GRCh38
NC_000009.11:g.139391809G>C , CM000671.1:g.139391809G>C	GRCh37
NC_000009.10:g.138511630G>C	NCBI36
NG_007458.1:g.53430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6382C>G MANE Select	ENSP00000498587.1:p.Pro2128Ala
ENST00000679595.1:c.*1422C>G	ENSP00000506241.1:n.*1422C>G
ENST00000679969.1:n.2978C>G
ENST00000680003.1:n.2714C>G
ENST00000680133.1:c.6268C>G	ENSP00000505319.1:p.Pro2090Ala
ENST00000680218.1:c.6262C>G	ENSP00000505339.1:p.Pro2088Ala
ENST00000680668.1:c.6268C>G	ENSP00000506336.1:p.Pro2090Ala
ENST00000680778.1:c.3979C>G	ENSP00000506033.1:p.Pro1327Ala
ENST00000680924.1:c.*3782C>G	ENSP00000506031.1:n.*3782C>G
ENST00000681135.1:c.*3991C>G	ENSP00000506636.1:n.*3991C>G
ENST00000681298.1:n.4487C>G
ENST00000681454.1:c.*5618C>G	ENSP00000505763.1:n.*5618C>G
ENST00000277541.6:c.6382C>G	ENSP00000277541.6:p.Pro2128Ala
NM_017617.3:c.6382C>G	NP_060087.3:p.Pro2128Ala
XM_011518717.1:c.5683C>G	XP_011517019.1:p.Pro1895Ala
NM_017617.5:c.6382C>G MANE Select	NP_060087.3:p.Pro2128Ala
XM_011518717.2:c.5659C>G	XP_011517019.2:p.Pro1887Ala