Canonical Allele Identifier: CA2080959269
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342160G= , CM000675.2:g.28342160G= GRCh38
NC_000013.10:g.28916297G= , CM000675.1:g.28916297G= GRCh37
NC_000013.9:g.27814297G= NCBI36
NG_012003.1:g.157969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706527.1:n.181-2860C=
ENST00000282397.9:c.2356-2860C= MANE Select ENSP00000282397.4:n.2356-2860C=
ENST00000282397.8:c.2356-2860C= ENSP00000282397.4:n.2356-2860C=
ENST00000540678.2:c.-1404-2860C= ENSP00000443311.2:n.-1404-2860C=
NM_002019.4:c.2356-2860C= MANE Select NP_002010.2:n.2356-2860C=
XM_017020485.1:c.2356-2860C= XP_016875974.1:n.2356-2860C=