Canonical Allele Identifier: CA362501870

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180046758C>G (hg19) ; chr5:g.180619758C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619758C>G , CM000667.2:g.180619758C>G	GRCh38
NC_000005.9:g.180046758C>G , CM000667.1:g.180046758C>G	GRCh37
NC_000005.8:g.179979364C>G	NCBI36
NG_011536.1:g.34867G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.2554G>C MANE Select	ENSP00000261937.6:p.Gly852Arg
ENST00000261937.10:c.2554G>C	ENSP00000261937.6:p.Gly852Arg
ENST00000393347.7:c.2554G>C	ENSP00000377016.3:p.Gly852Arg
ENST00000502649.5:c.2554G>C	ENSP00000426057.1:p.Gly852Arg
ENST00000507059.5:n.1649G>C
ENST00000619105.4:c.*1497G>C	ENSP00000481134.1:n.*1497G>C
NM_002020.4:c.2554G>C	NP_002011.2:p.Gly852Arg
NM_182925.4:c.2554G>C	NP_891555.2:p.Gly852Arg
XM_011534477.1:c.2803G>C	XP_011532779.1:p.Gly935Arg
XM_011534478.1:c.2785G>C	XP_011532780.1:p.Gly929Arg
XM_011534479.1:c.2803G>C	XP_011532781.1:p.Gly935Arg
XM_011534480.1:c.2803G>C	XP_011532782.1:p.Gly935Arg
XM_011534481.1:c.2803G>C	XP_011532783.1:p.Gly935Arg
XM_011534482.1:c.2572G>C	XP_011532784.1:p.Gly858Arg
XM_011534483.1:c.2494G>C	XP_011532785.1:p.Gly832Arg
XM_011534484.1:c.2095G>C	XP_011532786.1:p.Gly699Arg
XR_941095.1:n.2815G>C
NM_001354989.1:c.2554G>C	NP_001341918.1:p.Gly852Arg
XM_011534478.3:c.2785G>C	XP_011532780.1:p.Gly929Arg
XM_011534484.2:c.2095G>C	XP_011532786.1:p.Gly699Arg
XM_017009263.1:c.2785G>C	XP_016864752.1:p.Gly929Arg
XM_017009264.2:c.2785G>C	XP_016864753.1:p.Gly929Arg
XM_017009265.1:c.2785G>C	XP_016864754.1:p.Gly929Arg
XM_017009266.1:c.2785G>C	XP_016864755.1:p.Gly929Arg
XM_017009267.2:c.2785G>C	XP_016864756.1:p.Gly929Arg
XM_017009268.1:c.2476G>C	XP_016864757.1:p.Gly826Arg
XR_001742050.2:n.3019G>C
NM_182925.5:c.2554G>C MANE Select	NP_891555.2:p.Gly852Arg
NM_001354989.2:c.2554G>C	NP_001341918.1:p.Gly852Arg
NM_002020.5:c.2554G>C	NP_002011.2:p.Gly852Arg