Canonical Allele Identifier: CA404513145
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180120G>T , CM000681.2:g.15180120G>T GRCh38
NC_000019.9:g.15290931G>T , CM000681.1:g.15290931G>T GRCh37
NC_000019.8:g.15151931G>T NCBI36
NG_009819.1:g.25862C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3279C>A MANE Select ENSP00000263388.1:p.Cys1093Ter
ENST00000263388.6:c.3279C>A ENSP00000263388.1:p.Cys1093Ter
ENST00000601011.1:c.3120C>A ENSP00000473138.1:p.Cys1040Ter
NM_000435.2:c.3279C>A NP_000426.2:p.Cys1093Ter
XM_005259924.3:c.3123C>A XP_005259981.1:p.Cys1041Ter
XM_005259924.4:c.3123C>A XP_005259981.1:p.Cys1041Ter
NM_000435.3:c.3279C>A MANE Select NP_000426.2:p.Cys1093Ter