Canonical Allele Identifier: CA13783424

Gene: FLT1

Linked Data

• dbSNP Id: rs2387632
• gnomAD v2: 13-28916343-T-C
• gnomAD v3: 13-28342206-T-C
• gnomAD v4: 13-28342206-T-C
• MyVariant Identifiers: chr13:g.28916343T>C (hg19) ; chr13:g.28342206T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28342206T>C , CM000675.2:g.28342206T>C	GRCh38
NC_000013.10:g.28916343T>C , CM000675.1:g.28916343T>C	GRCh37
NC_000013.9:g.27814343T>C	NCBI36
NG_012003.1:g.157923A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706527.1:n.181-2906A>G
ENST00000282397.9:c.2356-2906A>G MANE Select	ENSP00000282397.4:n.2356-2906A>G
ENST00000282397.8:c.2356-2906A>G	ENSP00000282397.4:n.2356-2906A>G
ENST00000540678.2:c.-1404-2906A>G	ENSP00000443311.2:n.-1404-2906A>G
NM_002019.4:c.2356-2906A>G MANE Select	NP_002010.2:n.2356-2906A>G
XM_017020485.1:c.2356-2906A>G	XP_016875974.1:n.2356-2906A>G