Canonical Allele Identifier: CA13807614
Community Standard Title: NM_002019.4(FLT1):c.3286+575G>A
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28318848C>T , CM000675.2:g.28318848C>T GRCh38
NC_000013.10:g.28892985C>T , CM000675.1:g.28892985C>T GRCh37
NC_000013.9:g.27790985C>T NCBI36
NG_012003.1:g.181281G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002019.4:c.3286+575G>A MANE Select NP_002010.2:n.3286+575G>A
ENST00000282397.9:c.3286+575G>A MANE Select ENSP00000282397.4:n.3286+575G>A
ENST00000282397.8:c.3286+575G>A ENSP00000282397.4:n.3286+575G>A
ENST00000540678.2:c.-474+575G>A ENSP00000443311.2:n.-474+575G>A
ENST00000543394.2:c.355+575G>A ENSP00000437841.1:n.355+575G>A
ENST00000615611.4:c.571+575G>A ENSP00000484385.1:n.571+575G>A
ENST00000706527.1:n.1111+575G>A
XM_017020485.1:c.3172+575G>A XP_016875974.1:n.3172+575G>A
XR_941797.1:n.1237C>T
XR_941798.1:n.917+5068C>T