Canonical Allele Identifier: CA2080976234
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355523_28355524delinsCG , CM000675.2:g.28355523_28355524delinsCG GRCh38
NC_000013.10:g.28929660_28929661delinsCG , CM000675.1:g.28929660_28929661delinsCG GRCh37
NC_000013.9:g.27827660_27827661delinsCG NCBI36
NG_012003.1:g.144605_144606delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2030_2248+2031delinsCG MANE Select ENSP00000282397.4:n.2248+2030_2248+2031delinsCG
ENST00000282397.8:c.2248+2030_2248+2031delinsCG ENSP00000282397.4:n.2248+2030_2248+2031delinsCG
NM_002019.4:c.2248+2030_2248+2031delinsCG MANE Select NP_002010.2:n.2248+2030_2248+2031delinsCG
XM_017020485.1:c.2248+2030_2248+2031delinsCG XP_016875974.1:n.2248+2030_2248+2031delinsCG