Canonical Allele Identifier: CA2080976334
Gene: FLT1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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