Canonical Allele Identifier: CA247328729
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs559468084

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342183C>G , CM000675.2:g.28342183C>G GRCh38
NC_000013.10:g.28916320C>G , CM000675.1:g.28916320C>G GRCh37
NC_000013.9:g.27814320C>G NCBI36
NG_012003.1:g.157946G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706527.1:n.181-2883G>C
ENST00000282397.9:c.2356-2883G>C MANE Select ENSP00000282397.4:n.2356-2883G>C
ENST00000282397.8:c.2356-2883G>C ENSP00000282397.4:n.2356-2883G>C
ENST00000540678.2:c.-1404-2883G>C ENSP00000443311.2:n.-1404-2883G>C
NM_002019.4:c.2356-2883G>C MANE Select NP_002010.2:n.2356-2883G>C
XM_017020485.1:c.2356-2883G>C XP_016875974.1:n.2356-2883G>C