Canonical Allele Identifier: CA3605968
Gene: FLT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 263044
dbSNP Id: rs1130378

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180616388G>A , CM000667.2:g.180616388G>A GRCh38
NC_000005.9:g.180043388G>A , CM000667.1:g.180043388G>A GRCh37
NC_000005.8:g.179975994G>A NCBI36
NG_011536.1:g.38237C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261937.11:c.3198C>T MANE Select ENSP00000261937.6:p.Pro1066=
ENST00000261937.10:c.3198C>T ENSP00000261937.6:p.Pro1066=
ENST00000393347.7:c.3198C>T ENSP00000377016.3:p.Pro1066=
ENST00000502649.5:c.3198C>T ENSP00000426057.1:p.Pro1066=
ENST00000507059.5:n.2591C>T
ENST00000512795.1:c.312C>T ENSP00000421535.1:p.Pro104=
ENST00000514810.1:n.565C>T
ENST00000619105.4:c.*2141C>T ENSP00000481134.1:n.*2141C>T
NM_002020.4:c.3198C>T NP_002011.2:p.Pro1066=
NM_182925.4:c.3198C>T NP_891555.2:p.Pro1066=
XM_011534477.1:c.3447C>T XP_011532779.1:p.Pro1149=
XM_011534478.1:c.3429C>T XP_011532780.1:p.Pro1143=
XM_011534479.1:c.3447C>T XP_011532781.1:p.Pro1149=
XM_011534480.1:c.3447C>T XP_011532782.1:p.Pro1149=
XM_011534481.1:c.3447C>T XP_011532783.1:p.Pro1149=
XM_011534482.1:c.3216C>T XP_011532784.1:p.Pro1072=
XM_011534483.1:c.3138C>T XP_011532785.1:p.Pro1046=
XM_011534484.1:c.2739C>T XP_011532786.1:p.Pro913=
XR_941095.1:n.3459C>T
NM_001354989.1:c.3198C>T NP_001341918.1:p.Pro1066=
XM_011534478.3:c.3429C>T XP_011532780.1:p.Pro1143=
XM_011534484.2:c.2739C>T XP_011532786.1:p.Pro913=
XM_017009263.1:c.3429C>T XP_016864752.1:p.Pro1143=
XM_017009264.2:c.3429C>T XP_016864753.1:p.Pro1143=
XM_017009265.1:c.3429C>T XP_016864754.1:p.Pro1143=
XM_017009266.1:c.3429C>T XP_016864755.1:p.Pro1143=
XM_017009267.2:c.3429C>T XP_016864756.1:p.Pro1143=
XM_017009268.1:c.3120C>T XP_016864757.1:p.Pro1040=
XR_001742050.2:n.3663C>T
NM_182925.5:c.3198C>T MANE Select NP_891555.2:p.Pro1066=
NM_001354989.2:c.3198C>T NP_001341918.1:p.Pro1066=
NM_002020.5:c.3198C>T NP_002011.2:p.Pro1066=