Canonical Allele Identifier: CA2080976182
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355475A= , CM000675.2:g.28355475A= GRCh38
NC_000013.10:g.28929612A= , CM000675.1:g.28929612A= GRCh37
NC_000013.9:g.27827612A= NCBI36
NG_012003.1:g.144654T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2079T= MANE Select ENSP00000282397.4:n.2248+2079T=
ENST00000282397.8:c.2248+2079T= ENSP00000282397.4:n.2248+2079T=
NM_002019.4:c.2248+2079T= MANE Select NP_002010.2:n.2248+2079T=
XM_017020485.1:c.2248+2079T= XP_016875974.1:n.2248+2079T=