Canonical Allele Identifier: CA2580086888
Community Standard Title: NM_002019.4(FLT1):c.3174+225T>G
Gene: FLT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28321238A>C , CM000675.2:g.28321238A>C GRCh38
NC_000013.10:g.28895375A>C , CM000675.1:g.28895375A>C GRCh37
NC_000013.9:g.27793375A>C NCBI36
NG_012003.1:g.178891T>G

Transcript Alleles

HGVS Amino-acid Change
NM_002019.4:c.3174+225T>G MANE Select NP_002010.2:n.3174+225T>G
ENST00000282397.9:c.3174+225T>G MANE Select ENSP00000282397.4:n.3174+225T>G
ENST00000282397.8:c.3174+225T>G ENSP00000282397.4:n.3174+225T>G
ENST00000540678.2:c.-586+225T>G ENSP00000443311.2:n.-586+225T>G
ENST00000543394.2:c.243+225T>G ENSP00000437841.1:n.243+225T>G
ENST00000615611.4:c.459+225T>G ENSP00000484385.1:n.459+225T>G
ENST00000706527.1:n.999+225T>G
XM_017020485.1:c.3060+225T>G XP_016875974.1:n.3060+225T>G
XR_941798.1:n.918-7383A>C