Canonical Allele Identifier: CA404513472

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15290974C>G (hg19) ; chr19:g.15180163C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180163C>G , CM000681.2:g.15180163C>G	GRCh38
NC_000019.9:g.15290974C>G , CM000681.1:g.15290974C>G	GRCh37
NC_000019.8:g.15151974C>G	NCBI36
NG_009819.1:g.25819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.3236G>C MANE Select	ENSP00000263388.1:p.Ser1079Thr
ENST00000263388.6:c.3236G>C	ENSP00000263388.1:p.Ser1079Thr
ENST00000601011.1:c.3077G>C	ENSP00000473138.1:p.Ser1026Thr
NM_000435.2:c.3236G>C	NP_000426.2:p.Ser1079Thr
XM_005259924.3:c.3080G>C	XP_005259981.1:p.Ser1027Thr
XM_005259924.4:c.3080G>C	XP_005259981.1:p.Ser1027Thr
NM_000435.3:c.3236G>C MANE Select	NP_000426.2:p.Ser1079Thr