Canonical Allele Identifier: CA2080959247
Gene: FLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342144A= , CM000675.2:g.28342144A= GRCh38
NC_000013.10:g.28916281A= , CM000675.1:g.28916281A= GRCh37
NC_000013.9:g.27814281A= NCBI36
NG_012003.1:g.157985T=

Transcript Alleles

HGVS Amino-acid change
ENST00000706527.1:n.181-2844T=
ENST00000282397.9:c.2356-2844T= MANE Select ENSP00000282397.4:n.2356-2844T=
ENST00000282397.8:c.2356-2844T= ENSP00000282397.4:n.2356-2844T=
ENST00000540678.2:c.-1404-2844T= ENSP00000443311.2:n.-1404-2844T=
NM_002019.4:c.2356-2844T= MANE Select NP_002010.2:n.2356-2844T=
XM_017020485.1:c.2356-2844T= XP_016875974.1:n.2356-2844T=
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