Canonical Allele Identifier: CA2080976320
Gene: FLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355605G= , CM000675.2:g.28355605G= GRCh38
NC_000013.10:g.28929742G= , CM000675.1:g.28929742G= GRCh37
NC_000013.9:g.27827742G= NCBI36
NG_012003.1:g.144524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+1949C= MANE Select ENSP00000282397.4:n.2248+1949C=
ENST00000282397.8:c.2248+1949C= ENSP00000282397.4:n.2248+1949C=
NM_002019.4:c.2248+1949C= MANE Select NP_002010.2:n.2248+1949C=
XM_017020485.1:c.2248+1949C= XP_016875974.1:n.2248+1949C=
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