Canonical Allele Identifier: CA3605617

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603322C>T , CM000667.2:g.180603322C>T	GRCh38
NC_000005.9:g.180030322C>T , CM000667.1:g.180030322C>T	GRCh37
NC_000005.8:g.179962928C>T	NCBI36
NG_011536.1:g.51303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3962G>A MANE Select	ENSP00000261937.6:p.Arg1321Gln
ENST00000261937.10:c.3962G>A	ENSP00000261937.6:p.Arg1321Gln
ENST00000502603.5:n.662G>A
NM_182925.4:c.3962G>A	NP_891555.2:p.Arg1321Gln
XM_011534477.1:c.4211G>A	XP_011532779.1:p.Arg1404Gln
XM_011534478.1:c.4193G>A	XP_011532780.1:p.Arg1398Gln
XM_011534479.1:c.*108G>A	XP_011532781.1:n.*108G>A
XM_011534482.1:c.3980G>A	XP_011532784.1:p.Arg1327Gln
XM_011534483.1:c.3902G>A	XP_011532785.1:p.Arg1301Gln
XM_011534484.1:c.3503G>A	XP_011532786.1:p.Arg1168Gln
XR_941095.1:n.4248G>A
XM_011534478.3:c.4193G>A	XP_011532780.1:p.Arg1398Gln
XM_011534484.2:c.3503G>A	XP_011532786.1:p.Arg1168Gln
XM_017009263.1:c.*108G>A	XP_016864752.1:n.*108G>A
XM_017009268.1:c.3884G>A	XP_016864757.1:p.Arg1295Gln
XR_001742050.2:n.4452G>A
NM_182925.5:c.3962G>A MANE Select	NP_891555.2:p.Arg1321Gln