Canonical Allele Identifier: CA2581974321
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187468_15187469insCGGG , CM000681.2:g.15187468_15187469insCGGG GRCh38
NC_000019.9:g.15298279_15298280insCGGG , CM000681.1:g.15298279_15298280insCGGG GRCh37
NC_000019.8:g.15159279_15159280insCGGG NCBI36
NG_009819.1:g.18513_18514insCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-131_1607-130insCCCG MANE Select ENSP00000263388.1:n.1607-131_1607-130insCCCG
ENST00000263388.6:c.1607-131_1607-130insCCCG ENSP00000263388.1:n.1607-131_1607-130insCCCG
ENST00000601011.1:c.1604-131_1604-130insCCCG ENSP00000473138.1:n.1604-131_1604-130insCCCG
NM_000435.2:c.1607-131_1607-130insCCCG NP_000426.2:n.1607-131_1607-130insCCCG
XM_005259924.3:c.1607-131_1607-130insCCCG XP_005259981.1:n.1607-131_1607-130insCCCG
XM_005259924.4:c.1607-131_1607-130insCCCG XP_005259981.1:n.1607-131_1607-130insCCCG
NM_000435.3:c.1607-131_1607-130insCCCG MANE Select NP_000426.2:n.1607-131_1607-130insCCCG