Canonical Allele Identifier: CA2676967810
Gene: FLT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603466_180603467insTG , CM000667.2:g.180603466_180603467insTG GRCh38
NC_000005.9:g.180030466_180030467insTG , CM000667.1:g.180030466_180030467insTG GRCh37
NC_000005.8:g.179963072_179963073insTG NCBI36
NG_011536.1:g.51158_51159insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3894-77_3894-76insCA MANE Select ENSP00000261937.6:n.3894-77_3894-76insCA
ENST00000261937.10:c.3894-77_3894-76insCA ENSP00000261937.6:n.3894-77_3894-76insCA
ENST00000502603.5:n.594-77_594-76insCA
NM_182925.4:c.3894-77_3894-76insCA NP_891555.2:n.3894-77_3894-76insCA
XM_011534477.1:c.4143-77_4143-76insCA XP_011532779.1:n.4143-77_4143-76insCA
XM_011534478.1:c.4125-77_4125-76insCA XP_011532780.1:n.4125-77_4125-76insCA
XM_011534479.1:c.*40-77_*40-76insCA XP_011532781.1:n.*40-77_*40-76insCA
XM_011534482.1:c.3912-77_3912-76insCA XP_011532784.1:n.3912-77_3912-76insCA
XM_011534483.1:c.3834-77_3834-76insCA XP_011532785.1:n.3834-77_3834-76insCA
XM_011534484.1:c.3435-77_3435-76insCA XP_011532786.1:n.3435-77_3435-76insCA
XR_941095.1:n.4180-77_4180-76insCA
XM_011534478.3:c.4125-77_4125-76insCA XP_011532780.1:n.4125-77_4125-76insCA
XM_011534484.2:c.3435-77_3435-76insCA XP_011532786.1:n.3435-77_3435-76insCA
XM_017009263.1:c.*40-77_*40-76insCA XP_016864752.1:n.*40-77_*40-76insCA
XM_017009268.1:c.3816-77_3816-76insCA XP_016864757.1:n.3816-77_3816-76insCA
XR_001742050.2:n.4384-77_4384-76insCA
NM_182925.5:c.3894-77_3894-76insCA MANE Select NP_891555.2:n.3894-77_3894-76insCA