Canonical Allele Identifier: CA808402510
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs1462829473

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180614010T>C , CM000667.2:g.180614010T>C GRCh38
NC_000005.9:g.180041010T>C , CM000667.1:g.180041010T>C GRCh37
NC_000005.8:g.179973616T>C NCBI36
NG_011536.1:g.40615A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3331+58A>G MANE Select ENSP00000261937.6:n.3331+58A>G
ENST00000261937.10:c.3331+58A>G ENSP00000261937.6:n.3331+58A>G
ENST00000393347.7:c.3331+58A>G ENSP00000377016.3:n.3331+58A>G
ENST00000502649.5:c.3331+58A>G ENSP00000426057.1:n.3331+58A>G
ENST00000507059.5:n.2782A>G
ENST00000619105.4:c.*2274+58A>G ENSP00000481134.1:n.*2274+58A>G
NM_002020.4:c.3331+58A>G NP_002011.2:n.3331+58A>G
NM_182925.4:c.3331+58A>G NP_891555.2:n.3331+58A>G
XM_011534477.1:c.3580+58A>G XP_011532779.1:n.3580+58A>G
XM_011534478.1:c.3562+58A>G XP_011532780.1:n.3562+58A>G
XM_011534479.1:c.3580+58A>G XP_011532781.1:n.3580+58A>G
XM_011534480.1:c.3580+58A>G XP_011532782.1:n.3580+58A>G
XM_011534481.1:c.3580+58A>G XP_011532783.1:n.3580+58A>G
XM_011534482.1:c.3349+58A>G XP_011532784.1:n.3349+58A>G
XM_011534483.1:c.3271+58A>G XP_011532785.1:n.3271+58A>G
XM_011534484.1:c.2872+58A>G XP_011532786.1:n.2872+58A>G
XR_941095.1:n.3592+58A>G
NM_001354989.1:c.3331+58A>G NP_001341918.1:n.3331+58A>G
XM_011534478.3:c.3562+58A>G XP_011532780.1:n.3562+58A>G
XM_011534484.2:c.2872+58A>G XP_011532786.1:n.2872+58A>G
XM_017009263.1:c.3562+58A>G XP_016864752.1:n.3562+58A>G
XM_017009264.2:c.3562+58A>G XP_016864753.1:n.3562+58A>G
XM_017009265.1:c.3562+58A>G XP_016864754.1:n.3562+58A>G
XM_017009266.1:c.3562+58A>G XP_016864755.1:n.3562+58A>G
XM_017009267.2:c.3562+58A>G XP_016864756.1:n.3562+58A>G
XM_017009268.1:c.3253+58A>G XP_016864757.1:n.3253+58A>G
XR_001742050.2:n.3796+58A>G
NM_182925.5:c.3331+58A>G MANE Select NP_891555.2:n.3331+58A>G
NM_001354989.2:c.3331+58A>G NP_001341918.1:n.3331+58A>G
NM_002020.5:c.3331+58A>G NP_002011.2:n.3331+58A>G