Canonical Allele Identifier: CA3605592

Gene: FLT4

Linked Data

• dbSNP Id: rs754829541
• ExAC: 5:180030249 C / T
• gnomAD v2: 5-180030249-C-T
• gnomAD v3: 5-180603249-C-T
• gnomAD v4: 5-180603249-C-T
• MyVariant Identifiers: chr5:g.180030249C>T (hg19) ; chr5:g.180603249C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603249C>T , CM000667.2:g.180603249C>T	GRCh38
NC_000005.9:g.180030249C>T , CM000667.1:g.180030249C>T	GRCh37
NC_000005.8:g.179962855C>T	NCBI36
NG_011536.1:g.51376G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4035G>A MANE Select	ENSP00000261937.6:p.Glu1345=
ENST00000261937.10:c.4035G>A	ENSP00000261937.6:p.Glu1345=
ENST00000502603.5:n.735G>A
NM_182925.4:c.4035G>A	NP_891555.2:p.Glu1345=
XM_011534477.1:c.4284G>A	XP_011532779.1:p.Glu1428=
XM_011534478.1:c.4266G>A	XP_011532780.1:p.Glu1422=
XM_011534482.1:c.4053G>A	XP_011532784.1:p.Glu1351=
XM_011534483.1:c.3975G>A	XP_011532785.1:p.Glu1325=
XM_011534484.1:c.3576G>A	XP_011532786.1:p.Glu1192=
XR_941095.1:n.4321G>A
XM_011534478.3:c.4266G>A	XP_011532780.1:p.Glu1422=
XM_011534484.2:c.3576G>A	XP_011532786.1:p.Glu1192=
XM_017009263.1:c.*181G>A	XP_016864752.1:n.*181G>A
XM_017009268.1:c.3957G>A	XP_016864757.1:p.Glu1319=
XR_001742050.2:n.4525G>A
NM_182925.5:c.4035G>A MANE Select	NP_891555.2:p.Glu1345=