Canonical Allele Identifier: CA11992424
Gene: FLT4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10085109

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180633804G>C , CM000667.2:g.180633804G>C GRCh38
NC_000005.9:g.180060804G>C , CM000667.1:g.180060804G>C GRCh37
NC_000005.8:g.179993410G>C NCBI36
NG_011536.1:g.20821C>G

Transcript Alleles

HGVS Amino-acid change
NM_002020.4:c.59-2026C>G VV NP_002011.2:p.=
NM_182925.4:c.59-2026C>G VV NP_891555.2:p.=
XM_011534477.1:c.290-2026C>G XP_011532779.1:p.=
XM_011534478.1:c.290-2026C>G XP_011532780.1:p.=
XM_011534479.1:c.290-2026C>G XP_011532781.1:p.=
XM_011534480.1:c.290-2026C>G XP_011532782.1:p.=
XM_011534481.1:c.290-2026C>G XP_011532783.1:p.=
XM_011534482.1:c.59-2026C>G XP_011532784.1:p.=
XM_011534483.1:c.-20-2026C>G XP_011532785.1:p.=
XR_941095.1:n.302-2026C>G
NM_001354989.1:c.59-2026C>G VV NP_001341918.1:p.=
XM_011534478.3:c.290-2026C>G
XM_017009263.1:c.290-2026C>G XP_016864752.1:p.=
XM_017009264.2:c.290-2026C>G XP_016864753.1:p.=
XM_017009265.1:c.290-2026C>G XP_016864754.1:p.=
XM_017009266.1:c.290-2026C>G XP_016864755.1:p.=
XM_017009267.2:c.290-2026C>G XP_016864756.1:p.=
XM_017009268.1:c.-20-2026C>G XP_016864757.1:p.=
XR_001742050.2:n.524-2026C>G
ENST00000261937.10:c.59-2026C>G ENSP00000261937.6:p.=
ENST00000393347.7:c.59-2026C>G ENSP00000377016.3:p.=
ENST00000424276.6:n.59-2026C>G
ENST00000502293.5:n.59-2026C>G
ENST00000502649.5:c.59-2026C>G ENSP00000426057.1:p.=
ENST00000513527.1:n.59-2026C>G
ENST00000619105.4:c.59-2026C>G ENSP00000481134.1:p.=