Canonical Allele Identifier: CA2080976222
Gene: FLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355514T= , CM000675.2:g.28355514T= GRCh38
NC_000013.10:g.28929651T= , CM000675.1:g.28929651T= GRCh37
NC_000013.9:g.27827651T= NCBI36
NG_012003.1:g.144615A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2040A= MANE Select ENSP00000282397.4:n.2248+2040A=
ENST00000282397.8:c.2248+2040A= ENSP00000282397.4:n.2248+2040A=
NM_002019.4:c.2248+2040A= MANE Select NP_002010.2:n.2248+2040A=
XM_017020485.1:c.2248+2040A= XP_016875974.1:n.2248+2040A=
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