Canonical Allele Identifier: CA448103178

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180041150A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614150A>C , CM000667.2:g.180614150A>C	GRCh38
NC_000005.9:g.180041150A>C , CM000667.1:g.180041150A>C	GRCh37
NC_000005.8:g.179973756A>C	NCBI36
NG_011536.1:g.40475T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.3249T>G MANE Select	ENSP00000261937.6:p.Pro1083=
ENST00000261937.10:c.3249T>G	ENSP00000261937.6:p.Pro1083=
ENST00000393347.7:c.3249T>G	ENSP00000377016.3:p.Pro1083=
ENST00000502649.5:c.3249T>G	ENSP00000426057.1:p.Pro1083=
ENST00000507059.5:n.2642T>G
ENST00000512795.1:c.363T>G	ENSP00000421535.1:p.Pro121=
ENST00000514810.1:n.616T>G
ENST00000619105.4:c.*2192T>G	ENSP00000481134.1:n.*2192T>G
NM_002020.4:c.3249T>G	NP_002011.2:p.Pro1083=
NM_182925.4:c.3249T>G	NP_891555.2:p.Pro1083=
XM_011534477.1:c.3498T>G	XP_011532779.1:p.Pro1166=
XM_011534478.1:c.3480T>G	XP_011532780.1:p.Pro1160=
XM_011534479.1:c.3498T>G	XP_011532781.1:p.Pro1166=
XM_011534480.1:c.3498T>G	XP_011532782.1:p.Pro1166=
XM_011534481.1:c.3498T>G	XP_011532783.1:p.Pro1166=
XM_011534482.1:c.3267T>G	XP_011532784.1:p.Pro1089=
XM_011534483.1:c.3189T>G	XP_011532785.1:p.Pro1063=
XM_011534484.1:c.2790T>G	XP_011532786.1:p.Pro930=
XR_941095.1:n.3510T>G
NM_001354989.1:c.3249T>G	NP_001341918.1:p.Pro1083=
XM_011534478.3:c.3480T>G	XP_011532780.1:p.Pro1160=
XM_011534484.2:c.2790T>G	XP_011532786.1:p.Pro930=
XM_017009263.1:c.3480T>G	XP_016864752.1:p.Pro1160=
XM_017009264.2:c.3480T>G	XP_016864753.1:p.Pro1160=
XM_017009265.1:c.3480T>G	XP_016864754.1:p.Pro1160=
XM_017009266.1:c.3480T>G	XP_016864755.1:p.Pro1160=
XM_017009267.2:c.3480T>G	XP_016864756.1:p.Pro1160=
XM_017009268.1:c.3171T>G	XP_016864757.1:p.Pro1057=
XR_001742050.2:n.3714T>G
NM_182925.5:c.3249T>G MANE Select	NP_891555.2:p.Pro1083=
NM_001354989.2:c.3249T>G	NP_001341918.1:p.Pro1083=
NM_002020.5:c.3249T>G	NP_002011.2:p.Pro1083=