Canonical Allele Identifier: CA448105948

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180046756G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619756G>A , CM000667.2:g.180619756G>A	GRCh38
NC_000005.9:g.180046756G>A , CM000667.1:g.180046756G>A	GRCh37
NC_000005.8:g.179979362G>A	NCBI36
NG_011536.1:g.34869C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.2556C>T MANE Select	ENSP00000261937.6:p.Gly852=
ENST00000261937.10:c.2556C>T	ENSP00000261937.6:p.Gly852=
ENST00000393347.7:c.2556C>T	ENSP00000377016.3:p.Gly852=
ENST00000502649.5:c.2556C>T	ENSP00000426057.1:p.Gly852=
ENST00000507059.5:n.1651C>T
ENST00000619105.4:c.*1499C>T	ENSP00000481134.1:n.*1499C>T
NM_002020.4:c.2556C>T	NP_002011.2:p.Gly852=
NM_182925.4:c.2556C>T	NP_891555.2:p.Gly852=
XM_011534477.1:c.2805C>T	XP_011532779.1:p.Gly935=
XM_011534478.1:c.2787C>T	XP_011532780.1:p.Gly929=
XM_011534479.1:c.2805C>T	XP_011532781.1:p.Gly935=
XM_011534480.1:c.2805C>T	XP_011532782.1:p.Gly935=
XM_011534481.1:c.2805C>T	XP_011532783.1:p.Gly935=
XM_011534482.1:c.2574C>T	XP_011532784.1:p.Gly858=
XM_011534483.1:c.2496C>T	XP_011532785.1:p.Gly832=
XM_011534484.1:c.2097C>T	XP_011532786.1:p.Gly699=
XR_941095.1:n.2817C>T
NM_001354989.1:c.2556C>T	NP_001341918.1:p.Gly852=
XM_011534478.3:c.2787C>T	XP_011532780.1:p.Gly929=
XM_011534484.2:c.2097C>T	XP_011532786.1:p.Gly699=
XM_017009263.1:c.2787C>T	XP_016864752.1:p.Gly929=
XM_017009264.2:c.2787C>T	XP_016864753.1:p.Gly929=
XM_017009265.1:c.2787C>T	XP_016864754.1:p.Gly929=
XM_017009266.1:c.2787C>T	XP_016864755.1:p.Gly929=
XM_017009267.2:c.2787C>T	XP_016864756.1:p.Gly929=
XM_017009268.1:c.2478C>T	XP_016864757.1:p.Gly826=
XR_001742050.2:n.3021C>T
NM_182925.5:c.2556C>T MANE Select	NP_891555.2:p.Gly852=
NM_001354989.2:c.2556C>T	NP_001341918.1:p.Gly852=
NM_002020.5:c.2556C>T	NP_002011.2:p.Gly852=