Canonical Allele Identifier: CA404513028

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15290913G>T (hg19) ; chr19:g.15180102G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180102G>T , CM000681.2:g.15180102G>T	GRCh38
NC_000019.9:g.15290913G>T , CM000681.1:g.15290913G>T	GRCh37
NC_000019.8:g.15151913G>T	NCBI36
NG_009819.1:g.25880C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.3297C>A MANE Select	ENSP00000263388.1:p.Cys1099Ter
ENST00000263388.6:c.3297C>A	ENSP00000263388.1:p.Cys1099Ter
ENST00000601011.1:c.3138C>A	ENSP00000473138.1:p.Cys1046Ter
NM_000435.2:c.3297C>A	NP_000426.2:p.Cys1099Ter
XM_005259924.3:c.3141C>A	XP_005259981.1:p.Cys1047Ter
XM_005259924.4:c.3141C>A	XP_005259981.1:p.Cys1047Ter
NM_000435.3:c.3297C>A MANE Select	NP_000426.2:p.Cys1099Ter