Canonical Allele Identifier: CA2501741884
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355615G>T , CM000675.2:g.28355615G>T GRCh38
NC_000013.10:g.28929752G>T , CM000675.1:g.28929752G>T GRCh37
NC_000013.9:g.27827752G>T NCBI36
NG_012003.1:g.144514C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+1939C>A MANE Select ENSP00000282397.4:n.2248+1939C>A
ENST00000282397.8:c.2248+1939C>A ENSP00000282397.4:n.2248+1939C>A
NM_002019.4:c.2248+1939C>A MANE Select NP_002010.2:n.2248+1939C>A
XM_017020485.1:c.2248+1939C>A XP_016875974.1:n.2248+1939C>A