Canonical Allele Identifier: CA404534109
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145442256

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192211A>G , CM000681.2:g.15192211A>G GRCh38
NC_000019.9:g.15303022A>G , CM000681.1:g.15303022A>G GRCh37
NC_000019.8:g.15164022A>G NCBI36
NG_009819.1:g.13771T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.428T>C MANE Select ENSP00000263388.1:p.Leu143Pro
ENST00000263388.6:c.428T>C ENSP00000263388.1:p.Leu143Pro
ENST00000601011.1:c.425T>C ENSP00000473138.1:p.Leu142Pro
NM_000435.2:c.428T>C NP_000426.2:p.Leu143Pro
XM_005259924.3:c.428T>C XP_005259981.1:p.Leu143Pro
XM_005259924.4:c.428T>C XP_005259981.1:p.Leu143Pro
NM_000435.3:c.428T>C MANE Select NP_000426.2:p.Leu143Pro