Canonical Allele Identifier: CA404513298

Gene: NOTCH3

Linked Data

• dbSNP Id: rs1599381546
• MyVariant Identifiers: chr19:g.15290953T>G (hg19) ; chr19:g.15180142T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180142T>G , CM000681.2:g.15180142T>G	GRCh38
NC_000019.9:g.15290953T>G , CM000681.1:g.15290953T>G	GRCh37
NC_000019.8:g.15151953T>G	NCBI36
NG_009819.1:g.25840A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.3257A>C MANE Select	ENSP00000263388.1:p.Asp1086Ala
ENST00000263388.6:c.3257A>C	ENSP00000263388.1:p.Asp1086Ala
ENST00000601011.1:c.3098A>C	ENSP00000473138.1:p.Asp1033Ala
NM_000435.2:c.3257A>C	NP_000426.2:p.Asp1086Ala
XM_005259924.3:c.3101A>C	XP_005259981.1:p.Asp1034Ala
XM_005259924.4:c.3101A>C	XP_005259981.1:p.Asp1034Ala
NM_000435.3:c.3257A>C MANE Select	NP_000426.2:p.Asp1086Ala