Canonical Allele Identifier: CA375562992

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139412258T>C (hg19) ; chr9:g.136517806T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136517806T>C , CM000671.2:g.136517806T>C	GRCh38
NC_000009.11:g.139412258T>C , CM000671.1:g.139412258T>C	GRCh37
NC_000009.10:g.138532079T>C	NCBI36
NG_007458.1:g.32981A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.1387A>G MANE Select	ENSP00000498587.1:p.Asn463Asp
ENST00000679595.1:c.1387A>G	ENSP00000506241.1:p.Asn463Asp
ENST00000680133.1:c.1387A>G	ENSP00000505319.1:p.Asn463Asp
ENST00000680218.1:c.1387A>G	ENSP00000505339.1:p.Asn463Asp
ENST00000680668.1:c.1387A>G	ENSP00000506336.1:p.Asn463Asp
ENST00000680924.1:c.1387A>G	ENSP00000506031.1:p.Asn463Asp
ENST00000681135.1:c.1387A>G	ENSP00000506636.1:p.Asn463Asp
ENST00000681454.1:c.*623A>G	ENSP00000505763.1:n.*623A>G
ENST00000277541.6:c.1387A>G	ENSP00000277541.6:p.Asn463Asp
NM_017617.3:c.1387A>G	NP_060087.3:p.Asn463Asp
XM_011518717.1:c.688A>G	XP_011517019.1:p.Asn230Asp
NM_017617.5:c.1387A>G MANE Select	NP_060087.3:p.Asn463Asp
XM_011518717.2:c.664A>G	XP_011517019.2:p.Asn222Asp