Canonical Allele Identifier: CA13807632

Gene: FLT1

Linked Data

• dbSNP Id: rs600640
• gnomAD v2: 13-29063969-G-A
• gnomAD v3: 13-28489832-G-A
• gnomAD v4: 13-28489832-G-A
• MyVariant Identifiers: chr13:g.29063969G>A (hg19) ; chr13:g.28489832G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28489832G>A , CM000675.2:g.28489832G>A	GRCh38
NC_000013.10:g.29063969G>A , CM000675.1:g.29063969G>A	GRCh37
NC_000013.9:g.27961969G>A	NCBI36
NG_012003.1:g.10297C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539099.2:c.64+4948C>T	ENSP00000442630.1:n.64+4948C>T
ENST00000615840.5:c.64+4948C>T	ENSP00000484039.1:n.64+4948C>T
ENST00000282397.9:c.64+4948C>T MANE Select	ENSP00000282397.4:n.64+4948C>T
ENST00000639477.1:c.64+4948C>T	ENSP00000491097.1:n.64+4948C>T
ENST00000282397.8:c.64+4948C>T	ENSP00000282397.4:n.64+4948C>T
ENST00000539099.1:c.64+4948C>T	ENSP00000442630.1:n.64+4948C>T
ENST00000541932.5:c.64+4948C>T	ENSP00000437631.1:n.64+4948C>T
ENST00000615840.4:c.64+4948C>T	ENSP00000484039.1:n.64+4948C>T
NM_001159920.1:c.64+4948C>T	NP_001153392.1:n.64+4948C>T
NM_001160030.1:c.64+4948C>T	NP_001153502.1:n.64+4948C>T
NM_001160031.1:c.64+4948C>T	NP_001153503.1:n.64+4948C>T
NM_002019.4:c.64+4948C>T MANE Select	NP_002010.2:n.64+4948C>T
XM_011535014.1:c.64+4948C>T	XP_011533316.1:n.64+4948C>T
XM_017020485.1:c.64+4948C>T	XP_016875974.1:n.64+4948C>T
NM_001159920.2:c.64+4948C>T	NP_001153392.1:n.64+4948C>T
NM_001160030.2:c.64+4948C>T	NP_001153502.1:n.64+4948C>T