Canonical Allele Identifier: CA362500140

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180041081C>G (hg19) ; chr5:g.180614081C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614081C>G , CM000667.2:g.180614081C>G	GRCh38
NC_000005.9:g.180041081C>G , CM000667.1:g.180041081C>G	GRCh37
NC_000005.8:g.179973687C>G	NCBI36
NG_011536.1:g.40544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3318G>C MANE Select	ENSP00000261937.6:p.Glu1106Asp
ENST00000261937.10:c.3318G>C	ENSP00000261937.6:p.Glu1106Asp
ENST00000393347.7:c.3318G>C	ENSP00000377016.3:p.Glu1106Asp
ENST00000502649.5:c.3318G>C	ENSP00000426057.1:p.Glu1106Asp
ENST00000507059.5:n.2711G>C
ENST00000514810.1:n.685G>C
ENST00000619105.4:c.*2261G>C	ENSP00000481134.1:n.*2261G>C
NM_002020.4:c.3318G>C	NP_002011.2:p.Glu1106Asp
NM_182925.4:c.3318G>C	NP_891555.2:p.Glu1106Asp
XM_011534477.1:c.3567G>C	XP_011532779.1:p.Glu1189Asp
XM_011534478.1:c.3549G>C	XP_011532780.1:p.Glu1183Asp
XM_011534479.1:c.3567G>C	XP_011532781.1:p.Glu1189Asp
XM_011534480.1:c.3567G>C	XP_011532782.1:p.Glu1189Asp
XM_011534481.1:c.3567G>C	XP_011532783.1:p.Glu1189Asp
XM_011534482.1:c.3336G>C	XP_011532784.1:p.Glu1112Asp
XM_011534483.1:c.3258G>C	XP_011532785.1:p.Glu1086Asp
XM_011534484.1:c.2859G>C	XP_011532786.1:p.Glu953Asp
XR_941095.1:n.3579G>C
NM_001354989.1:c.3318G>C	NP_001341918.1:p.Glu1106Asp
XM_011534478.3:c.3549G>C	XP_011532780.1:p.Glu1183Asp
XM_011534484.2:c.2859G>C	XP_011532786.1:p.Glu953Asp
XM_017009263.1:c.3549G>C	XP_016864752.1:p.Glu1183Asp
XM_017009264.2:c.3549G>C	XP_016864753.1:p.Glu1183Asp
XM_017009265.1:c.3549G>C	XP_016864754.1:p.Glu1183Asp
XM_017009266.1:c.3549G>C	XP_016864755.1:p.Glu1183Asp
XM_017009267.2:c.3549G>C	XP_016864756.1:p.Glu1183Asp
XM_017009268.1:c.3240G>C	XP_016864757.1:p.Glu1080Asp
XR_001742050.2:n.3783G>C
NM_182925.5:c.3318G>C MANE Select	NP_891555.2:p.Glu1106Asp
NM_001354989.2:c.3318G>C	NP_001341918.1:p.Glu1106Asp
NM_002020.5:c.3318G>C	NP_002011.2:p.Glu1106Asp