Canonical Allele Identifier: CA2080976246
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355527G= , CM000675.2:g.28355527G= GRCh38
NC_000013.10:g.28929664G= , CM000675.1:g.28929664G= GRCh37
NC_000013.9:g.27827664G= NCBI36
NG_012003.1:g.144602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2027C= MANE Select ENSP00000282397.4:n.2248+2027C=
ENST00000282397.8:c.2248+2027C= ENSP00000282397.4:n.2248+2027C=
NM_002019.4:c.2248+2027C= MANE Select NP_002010.2:n.2248+2027C=
XM_017020485.1:c.2248+2027C= XP_016875974.1:n.2248+2027C=