Canonical Allele Identifier: CA2080992372

Gene: FLT1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28410365G>C , CM000675.2:g.28410365G>C	GRCh38
NC_000013.10:g.28984502G>C , CM000675.1:g.28984502G>C	GRCh37
NC_000013.9:g.27882502G>C	NCBI36
NG_012003.1:g.89764C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539099.2:c.1437-4471C>G	ENSP00000442630.1:n.1437-4471C>G
ENST00000615840.5:c.1437-4471C>G	ENSP00000484039.1:n.1437-4471C>G
ENST00000282397.9:c.1437-4471C>G MANE Select	ENSP00000282397.4:n.1437-4471C>G
ENST00000639477.1:c.1437-4471C>G	ENSP00000491097.1:n.1437-4471C>G
ENST00000282397.8:c.1437-4471C>G	ENSP00000282397.4:n.1437-4471C>G
ENST00000539099.1:c.1437-4471C>G	ENSP00000442630.1:n.1437-4471C>G
ENST00000541932.5:c.1437-4471C>G	ENSP00000437631.1:n.1437-4471C>G
ENST00000615840.4:c.1437-4471C>G	ENSP00000484039.1:n.1437-4471C>G
NM_001159920.1:c.1437-4471C>G	NP_001153392.1:n.1437-4471C>G
NM_001160030.1:c.1437-4471C>G	NP_001153502.1:n.1437-4471C>G
NM_001160031.1:c.1437-4471C>G	NP_001153503.1:n.1437-4471C>G
NM_002019.4:c.1437-4471C>G MANE Select	NP_002010.2:n.1437-4471C>G
XM_011535014.1:c.1437-4471C>G	XP_011533316.1:n.1437-4471C>G
XM_017020485.1:c.1437-4471C>G	XP_016875974.1:n.1437-4471C>G
NM_001159920.2:c.1437-4471C>G	NP_001153392.1:n.1437-4471C>G
NM_001160030.2:c.1437-4471C>G	NP_001153502.1:n.1437-4471C>G