Canonical Allele Identifier: CA2583064856
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187482_15187483insCCCCCCCCCCTACC , CM000681.2:g.15187482_15187483insCCCCCCCCCCTACC GRCh38
NC_000019.9:g.15298293_15298294insCCCCCCCCCCTACC , CM000681.1:g.15298293_15298294insCCCCCCCCCCTACC GRCh37
NC_000019.8:g.15159293_15159294insCCCCCCCCCCTACC NCBI36
NG_009819.1:g.18501_18502insTAGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-143_1607-142insTAGGGGGGGGGGGG MANE Select ENSP00000263388.1:n.1607-143_1607-142insTAGGGGGGGGGGGG
ENST00000263388.6:c.1607-143_1607-142insTAGGGGGGGGGGGG ENSP00000263388.1:n.1607-143_1607-142insTAGGGGGGGGGGGG
ENST00000601011.1:c.1604-143_1604-142insTAGGGGGGGGGGGG ENSP00000473138.1:n.1604-143_1604-142insTAGGGGGGGGGGGG
NM_000435.2:c.1607-143_1607-142insTAGGGGGGGGGGGG NP_000426.2:n.1607-143_1607-142insTAGGGGGGGGGGGG
XM_005259924.3:c.1607-143_1607-142insTAGGGGGGGGGGGG XP_005259981.1:n.1607-143_1607-142insTAGGGGGGGGGGGG
XM_005259924.4:c.1607-143_1607-142insTAGGGGGGGGGGGG XP_005259981.1:n.1607-143_1607-142insTAGGGGGGGGGGGG
NM_000435.3:c.1607-143_1607-142insTAGGGGGGGGGGGG MANE Select NP_000426.2:n.1607-143_1607-142insTAGGGGGGGGGGGG