Canonical Allele Identifier: CA362497930

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036936G>C (hg19) ; chr5:g.180609936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609936G>C , CM000667.2:g.180609936G>C	GRCh38
NC_000005.9:g.180036936G>C , CM000667.1:g.180036936G>C	GRCh37
NC_000005.8:g.179969542G>C	NCBI36
NG_011536.1:g.44689C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3776C>G MANE Select	ENSP00000261937.6:p.Pro1259Arg
ENST00000261937.10:c.3776C>G	ENSP00000261937.6:p.Pro1259Arg
ENST00000393347.7:c.3776C>G	ENSP00000377016.3:p.Pro1259Arg
ENST00000502603.5:n.476C>G
ENST00000502649.5:c.3776C>G	ENSP00000426057.1:p.Pro1259Arg
ENST00000507059.5:n.4126C>G
ENST00000619105.4:c.*2719C>G	ENSP00000481134.1:n.*2719C>G
NM_002020.4:c.3776C>G	NP_002011.2:p.Pro1259Arg
NM_182925.4:c.3776C>G	NP_891555.2:p.Pro1259Arg
XM_011534477.1:c.4025C>G	XP_011532779.1:p.Pro1342Arg
XM_011534478.1:c.4007C>G	XP_011532780.1:p.Pro1336Arg
XM_011534479.1:c.4025C>G	XP_011532781.1:p.Pro1342Arg
XM_011534480.1:c.4025C>G	XP_011532782.1:p.Pro1342Arg
XM_011534481.1:c.4025C>G	XP_011532783.1:p.Pro1342Arg
XM_011534482.1:c.3794C>G	XP_011532784.1:p.Pro1265Arg
XM_011534483.1:c.3716C>G	XP_011532785.1:p.Pro1239Arg
XM_011534484.1:c.3317C>G	XP_011532786.1:p.Pro1106Arg
XR_941095.1:n.4062C>G
NM_001354989.1:c.3776C>G	NP_001341918.1:p.Pro1259Arg
XM_011534478.3:c.4007C>G	XP_011532780.1:p.Pro1336Arg
XM_011534484.2:c.3317C>G	XP_011532786.1:p.Pro1106Arg
XM_017009263.1:c.4007C>G	XP_016864752.1:p.Pro1336Arg
XM_017009264.2:c.4007C>G	XP_016864753.1:p.Pro1336Arg
XM_017009265.1:c.4007C>G	XP_016864754.1:p.Pro1336Arg
XM_017009266.1:c.4007C>G	XP_016864755.1:p.Pro1336Arg
XM_017009267.2:c.4007C>G	XP_016864756.1:p.Pro1336Arg
XM_017009268.1:c.3698C>G	XP_016864757.1:p.Pro1233Arg
XR_001742050.2:n.4266C>G
NM_182925.5:c.3776C>G MANE Select	NP_891555.2:p.Pro1259Arg
NM_001354989.2:c.3776C>G	NP_001341918.1:p.Pro1259Arg
NM_002020.5:c.3776C>G	NP_002011.2:p.Pro1259Arg