Canonical Allele Identifier: CA375645219

Gene: NOTCH1

Linked Data

• dbSNP Id: rs771357343
• MyVariant Identifiers: chr9:g.139399398G>T (hg19) ; chr9:g.136504946G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504946G>T , CM000671.2:g.136504946G>T	GRCh38
NC_000009.11:g.139399398G>T , CM000671.1:g.139399398G>T	GRCh37
NC_000009.10:g.138519219G>T	NCBI36
NG_007458.1:g.45841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2552C>A
ENST00000651671.1:c.4745C>A MANE Select	ENSP00000498587.1:p.Pro1582Gln
ENST00000679595.1:c.4745C>A	ENSP00000506241.1:p.Pro1582Gln
ENST00000680133.1:c.4631C>A	ENSP00000505319.1:p.Pro1544Gln
ENST00000680218.1:c.4625C>A	ENSP00000505339.1:p.Pro1542Gln
ENST00000680668.1:c.4631C>A	ENSP00000506336.1:p.Pro1544Gln
ENST00000680778.1:c.2342C>A	ENSP00000506033.1:p.Pro781Gln
ENST00000680924.1:c.*2145C>A	ENSP00000506031.1:n.*2145C>A
ENST00000681135.1:c.*2354C>A	ENSP00000506636.1:n.*2354C>A
ENST00000681298.1:n.1558C>A
ENST00000681454.1:c.*3981C>A	ENSP00000505763.1:n.*3981C>A
ENST00000277541.6:c.4745C>A	ENSP00000277541.6:p.Pro1582Gln
NM_017617.3:c.4745C>A	NP_060087.3:p.Pro1582Gln
XM_011518717.1:c.4046C>A	XP_011517019.1:p.Pro1349Gln
NM_017617.5:c.4745C>A MANE Select	NP_060087.3:p.Pro1582Gln
XM_011518717.2:c.4022C>A	XP_011517019.2:p.Pro1341Gln