Canonical Allele Identifier: CA3605588
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs201336964

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603244T>G , CM000667.2:g.180603244T>G GRCh38
NC_000005.9:g.180030244T>G , CM000667.1:g.180030244T>G GRCh37
NC_000005.8:g.179962850T>G NCBI36
NG_011536.1:g.51381A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.4040A>C MANE Select ENSP00000261937.6:p.Asp1347Ala
ENST00000261937.10:c.4040A>C ENSP00000261937.6:p.Asp1347Ala
ENST00000502603.5:n.740A>C
NM_182925.4:c.4040A>C NP_891555.2:p.Asp1347Ala
XM_011534477.1:c.4289A>C XP_011532779.1:p.Asp1430Ala
XM_011534478.1:c.4271A>C XP_011532780.1:p.Asp1424Ala
XM_011534482.1:c.4058A>C XP_011532784.1:p.Asp1353Ala
XM_011534483.1:c.3980A>C XP_011532785.1:p.Asp1327Ala
XM_011534484.1:c.3581A>C XP_011532786.1:p.Asp1194Ala
XR_941095.1:n.4326A>C
XM_011534478.3:c.4271A>C XP_011532780.1:p.Asp1424Ala
XM_011534484.2:c.3581A>C XP_011532786.1:p.Asp1194Ala
XM_017009263.1:c.*186A>C XP_016864752.1:n.*186A>C
XM_017009268.1:c.3962A>C XP_016864757.1:p.Asp1321Ala
XR_001742050.2:n.4530A>C
NM_182925.5:c.4040A>C MANE Select NP_891555.2:p.Asp1347Ala