Canonical Allele Identifier: CA362500278

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180041142A>C (hg19) ; chr5:g.180614142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614142A>C , CM000667.2:g.180614142A>C	GRCh38
NC_000005.9:g.180041142A>C , CM000667.1:g.180041142A>C	GRCh37
NC_000005.8:g.179973748A>C	NCBI36
NG_011536.1:g.40483T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.3257T>G MANE Select	ENSP00000261937.6:p.Ile1086Ser
ENST00000261937.10:c.3257T>G	ENSP00000261937.6:p.Ile1086Ser
ENST00000393347.7:c.3257T>G	ENSP00000377016.3:p.Ile1086Ser
ENST00000502649.5:c.3257T>G	ENSP00000426057.1:p.Ile1086Ser
ENST00000507059.5:n.2650T>G
ENST00000512795.1:c.371T>G	ENSP00000421535.1:p.Ile124Ser
ENST00000514810.1:n.624T>G
ENST00000619105.4:c.*2200T>G	ENSP00000481134.1:n.*2200T>G
NM_002020.4:c.3257T>G	NP_002011.2:p.Ile1086Ser
NM_182925.4:c.3257T>G	NP_891555.2:p.Ile1086Ser
XM_011534477.1:c.3506T>G	XP_011532779.1:p.Ile1169Ser
XM_011534478.1:c.3488T>G	XP_011532780.1:p.Ile1163Ser
XM_011534479.1:c.3506T>G	XP_011532781.1:p.Ile1169Ser
XM_011534480.1:c.3506T>G	XP_011532782.1:p.Ile1169Ser
XM_011534481.1:c.3506T>G	XP_011532783.1:p.Ile1169Ser
XM_011534482.1:c.3275T>G	XP_011532784.1:p.Ile1092Ser
XM_011534483.1:c.3197T>G	XP_011532785.1:p.Ile1066Ser
XM_011534484.1:c.2798T>G	XP_011532786.1:p.Ile933Ser
XR_941095.1:n.3518T>G
NM_001354989.1:c.3257T>G	NP_001341918.1:p.Ile1086Ser
XM_011534478.3:c.3488T>G	XP_011532780.1:p.Ile1163Ser
XM_011534484.2:c.2798T>G	XP_011532786.1:p.Ile933Ser
XM_017009263.1:c.3488T>G	XP_016864752.1:p.Ile1163Ser
XM_017009264.2:c.3488T>G	XP_016864753.1:p.Ile1163Ser
XM_017009265.1:c.3488T>G	XP_016864754.1:p.Ile1163Ser
XM_017009266.1:c.3488T>G	XP_016864755.1:p.Ile1163Ser
XM_017009267.2:c.3488T>G	XP_016864756.1:p.Ile1163Ser
XM_017009268.1:c.3179T>G	XP_016864757.1:p.Ile1060Ser
XR_001742050.2:n.3722T>G
NM_182925.5:c.3257T>G MANE Select	NP_891555.2:p.Ile1086Ser
NM_001354989.2:c.3257T>G	NP_001341918.1:p.Ile1086Ser
NM_002020.5:c.3257T>G	NP_002011.2:p.Ile1086Ser