Canonical Allele Identifier: CA2080959194
Gene: FLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342134C= , CM000675.2:g.28342134C= GRCh38
NC_000013.10:g.28916271C= , CM000675.1:g.28916271C= GRCh37
NC_000013.9:g.27814271C= NCBI36
NG_012003.1:g.157995G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706527.1:n.181-2834G=
ENST00000282397.9:c.2356-2834G= MANE Select ENSP00000282397.4:n.2356-2834G=
ENST00000282397.8:c.2356-2834G= ENSP00000282397.4:n.2356-2834G=
ENST00000540678.2:c.-1404-2834G= ENSP00000443311.2:n.-1404-2834G=
NM_002019.4:c.2356-2834G= MANE Select NP_002010.2:n.2356-2834G=
XM_017020485.1:c.2356-2834G= XP_016875974.1:n.2356-2834G=
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