Canonical Allele Identifier: CA448101356

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036935G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609935G>T , CM000667.2:g.180609935G>T	GRCh38
NC_000005.9:g.180036935G>T , CM000667.1:g.180036935G>T	GRCh37
NC_000005.8:g.179969541G>T	NCBI36
NG_011536.1:g.44690C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3777C>A MANE Select	ENSP00000261937.6:p.Pro1259=
ENST00000261937.10:c.3777C>A	ENSP00000261937.6:p.Pro1259=
ENST00000393347.7:c.3777C>A	ENSP00000377016.3:p.Pro1259=
ENST00000502603.5:n.477C>A
ENST00000502649.5:c.3777C>A	ENSP00000426057.1:p.Pro1259=
ENST00000507059.5:n.4127C>A
ENST00000619105.4:c.*2720C>A	ENSP00000481134.1:n.*2720C>A
NM_002020.4:c.3777C>A	NP_002011.2:p.Pro1259=
NM_182925.4:c.3777C>A	NP_891555.2:p.Pro1259=
XM_011534477.1:c.4026C>A	XP_011532779.1:p.Pro1342=
XM_011534478.1:c.4008C>A	XP_011532780.1:p.Pro1336=
XM_011534479.1:c.4026C>A	XP_011532781.1:p.Pro1342=
XM_011534480.1:c.4026C>A	XP_011532782.1:p.Pro1342=
XM_011534481.1:c.4026C>A	XP_011532783.1:p.Pro1342=
XM_011534482.1:c.3795C>A	XP_011532784.1:p.Pro1265=
XM_011534483.1:c.3717C>A	XP_011532785.1:p.Pro1239=
XM_011534484.1:c.3318C>A	XP_011532786.1:p.Pro1106=
XR_941095.1:n.4063C>A
NM_001354989.1:c.3777C>A	NP_001341918.1:p.Pro1259=
XM_011534478.3:c.4008C>A	XP_011532780.1:p.Pro1336=
XM_011534484.2:c.3318C>A	XP_011532786.1:p.Pro1106=
XM_017009263.1:c.4008C>A	XP_016864752.1:p.Pro1336=
XM_017009264.2:c.4008C>A	XP_016864753.1:p.Pro1336=
XM_017009265.1:c.4008C>A	XP_016864754.1:p.Pro1336=
XM_017009266.1:c.4008C>A	XP_016864755.1:p.Pro1336=
XM_017009267.2:c.4008C>A	XP_016864756.1:p.Pro1336=
XM_017009268.1:c.3699C>A	XP_016864757.1:p.Pro1233=
XR_001742050.2:n.4267C>A
NM_182925.5:c.3777C>A MANE Select	NP_891555.2:p.Pro1259=
NM_001354989.2:c.3777C>A	NP_001341918.1:p.Pro1259=
NM_002020.5:c.3777C>A	NP_002011.2:p.Pro1259=