Canonical Allele Identifier: CA993904805
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187475_15187476insCCCCCCCC , CM000681.2:g.15187475_15187476insCCCCCCCC GRCh38
NC_000019.9:g.15298286_15298287insCCCCCCCC , CM000681.1:g.15298286_15298287insCCCCCCCC GRCh37
NC_000019.8:g.15159286_15159287insCCCCCCCC NCBI36
NG_009819.1:g.18510_18511insGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-134_1607-133insGGGGGGGG MANE Select ENSP00000263388.1:n.1607-134_1607-133insGGGGGGGG
ENST00000263388.6:c.1607-134_1607-133insGGGGGGGG ENSP00000263388.1:n.1607-134_1607-133insGGGGGGGG
ENST00000601011.1:c.1604-134_1604-133insGGGGGGGG ENSP00000473138.1:n.1604-134_1604-133insGGGGGGGG
NM_000435.2:c.1607-134_1607-133insGGGGGGGG NP_000426.2:n.1607-134_1607-133insGGGGGGGG
XM_005259924.3:c.1607-134_1607-133insGGGGGGGG XP_005259981.1:n.1607-134_1607-133insGGGGGGGG
XM_005259924.4:c.1607-134_1607-133insGGGGGGGG XP_005259981.1:n.1607-134_1607-133insGGGGGGGG
NM_000435.3:c.1607-134_1607-133insGGGGGGGG MANE Select NP_000426.2:n.1607-134_1607-133insGGGGGGGG