Canonical Allele Identifier: CA15785762

Gene: FLT1

Linked Data

• dbSNP Id: rs722503
• gnomAD v2: 13-28997052-C-T
• gnomAD v3: 13-28422915-C-T
• gnomAD v4: 13-28422915-C-T
• MyVariant Identifiers: chr13:g.28997052C>T (hg19) ; chr13:g.28422915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28422915C>T , CM000675.2:g.28422915C>T	GRCh38
NC_000013.10:g.28997052C>T , CM000675.1:g.28997052C>T	GRCh37
NC_000013.9:g.27895052C>T	NCBI36
NG_012003.1:g.77214G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000539099.2:c.1436+4244G>A	ENSP00000442630.1:n.1436+4244G>A
ENST00000615840.5:c.1436+4244G>A	ENSP00000484039.1:n.1436+4244G>A
ENST00000282397.9:c.1436+4244G>A MANE Select	ENSP00000282397.4:n.1436+4244G>A
ENST00000639477.1:c.1436+4244G>A	ENSP00000491097.1:n.1436+4244G>A
ENST00000282397.8:c.1436+4244G>A	ENSP00000282397.4:n.1436+4244G>A
ENST00000539099.1:c.1436+4244G>A	ENSP00000442630.1:n.1436+4244G>A
ENST00000541932.5:c.1436+4244G>A	ENSP00000437631.1:n.1436+4244G>A
ENST00000615840.4:c.1436+4244G>A	ENSP00000484039.1:n.1436+4244G>A
NM_001159920.1:c.1436+4244G>A	NP_001153392.1:n.1436+4244G>A
NM_001160030.1:c.1436+4244G>A	NP_001153502.1:n.1436+4244G>A
NM_001160031.1:c.1436+4244G>A	NP_001153503.1:n.1436+4244G>A
NM_002019.4:c.1436+4244G>A MANE Select	NP_002010.2:n.1436+4244G>A
XM_011535014.1:c.1436+4244G>A	XP_011533316.1:n.1436+4244G>A
XM_017020485.1:c.1436+4244G>A	XP_016875974.1:n.1436+4244G>A
NM_001159920.2:c.1436+4244G>A	NP_001153392.1:n.1436+4244G>A
NM_001160030.2:c.1436+4244G>A	NP_001153502.1:n.1436+4244G>A