Canonical Allele Identifier: CA2080976232
Gene: FLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355523C= , CM000675.2:g.28355523C= GRCh38
NC_000013.10:g.28929660C= , CM000675.1:g.28929660C= GRCh37
NC_000013.9:g.27827660C= NCBI36
NG_012003.1:g.144606G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2031G= MANE Select ENSP00000282397.4:n.2248+2031G=
ENST00000282397.8:c.2248+2031G= ENSP00000282397.4:n.2248+2031G=
NM_002019.4:c.2248+2031G= MANE Select NP_002010.2:n.2248+2031G=
XM_017020485.1:c.2248+2031G= XP_016875974.1:n.2248+2031G=
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