Canonical Allele Identifier: CA362495567

Gene: FLT4

Linked Data

• dbSNP Id: rs781063816
• gnomAD v2: 5-180030251-C-G
• gnomAD v3: 5-180603251-C-G
• gnomAD v4: 5-180603251-C-G
• MyVariant Identifiers: chr5:g.180030251C>G (hg19) ; chr5:g.180603251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603251C>G , CM000667.2:g.180603251C>G	GRCh38
NC_000005.9:g.180030251C>G , CM000667.1:g.180030251C>G	GRCh37
NC_000005.8:g.179962857C>G	NCBI36
NG_011536.1:g.51374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4033G>C MANE Select	ENSP00000261937.6:p.Glu1345Gln
ENST00000261937.10:c.4033G>C	ENSP00000261937.6:p.Glu1345Gln
ENST00000502603.5:n.733G>C
NM_182925.4:c.4033G>C	NP_891555.2:p.Glu1345Gln
XM_011534477.1:c.4282G>C	XP_011532779.1:p.Glu1428Gln
XM_011534478.1:c.4264G>C	XP_011532780.1:p.Glu1422Gln
XM_011534482.1:c.4051G>C	XP_011532784.1:p.Glu1351Gln
XM_011534483.1:c.3973G>C	XP_011532785.1:p.Glu1325Gln
XM_011534484.1:c.3574G>C	XP_011532786.1:p.Glu1192Gln
XR_941095.1:n.4319G>C
XM_011534478.3:c.4264G>C	XP_011532780.1:p.Glu1422Gln
XM_011534484.2:c.3574G>C	XP_011532786.1:p.Glu1192Gln
XM_017009263.1:c.*179G>C	XP_016864752.1:n.*179G>C
XM_017009268.1:c.3955G>C	XP_016864757.1:p.Glu1319Gln
XR_001742050.2:n.4523G>C
NM_182925.5:c.4033G>C MANE Select	NP_891555.2:p.Glu1345Gln