Canonical Allele Identifier: CA3606016
Community Standard Title: NM_182925.5(FLT4):c.3023C>T (p.Pro1008Leu)
Gene: FLT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180616973G>A , CM000667.2:g.180616973G>A GRCh38
NC_000005.9:g.180043973G>A , CM000667.1:g.180043973G>A GRCh37
NC_000005.8:g.179976579G>A NCBI36
NG_011536.1:g.37652C>T

Transcript Alleles

HGVS Amino-acid Change
NM_182925.5:c.3023C>T MANE Select NP_891555.2:p.Pro1008Leu
ENST00000261937.11:c.3023C>T MANE Select ENSP00000261937.6:p.Pro1008Leu
NM_001354989.1:c.3023C>T NP_001341918.1:p.Pro1008Leu
NM_001354989.2:c.3023C>T NP_001341918.1:p.Pro1008Leu
NM_002020.4:c.3023C>T NP_002011.2:p.Pro1008Leu
NM_002020.5:c.3023C>T NP_002011.2:p.Pro1008Leu
NM_182925.4:c.3023C>T NP_891555.2:p.Pro1008Leu
ENST00000261937.10:c.3023C>T ENSP00000261937.6:p.Pro1008Leu
ENST00000393347.7:c.3023C>T ENSP00000377016.3:p.Pro1008Leu
ENST00000502649.5:c.3023C>T ENSP00000426057.1:p.Pro1008Leu
ENST00000507059.5:n.2416C>T
ENST00000512795.1:c.137C>T ENSP00000421535.1:p.Pro46Leu
ENST00000514810.1:n.390C>T
ENST00000619105.4:c.*1966C>T ENSP00000481134.1:n.*1966C>T
XM_011534477.1:c.3272C>T XP_011532779.1:p.Pro1091Leu
XM_011534478.1:c.3254C>T XP_011532780.1:p.Pro1085Leu
XM_011534478.3:c.3254C>T XP_011532780.1:p.Pro1085Leu
XM_011534479.1:c.3272C>T XP_011532781.1:p.Pro1091Leu
XM_011534480.1:c.3272C>T XP_011532782.1:p.Pro1091Leu
XM_011534481.1:c.3272C>T XP_011532783.1:p.Pro1091Leu
XM_011534482.1:c.3041C>T XP_011532784.1:p.Pro1014Leu
XM_011534483.1:c.2963C>T XP_011532785.1:p.Pro988Leu
XM_011534484.1:c.2564C>T XP_011532786.1:p.Pro855Leu
XM_011534484.2:c.2564C>T XP_011532786.1:p.Pro855Leu
XM_017009263.1:c.3254C>T XP_016864752.1:p.Pro1085Leu
XM_017009264.2:c.3254C>T XP_016864753.1:p.Pro1085Leu
XM_017009265.1:c.3254C>T XP_016864754.1:p.Pro1085Leu
XM_017009266.1:c.3254C>T XP_016864755.1:p.Pro1085Leu
XM_017009267.2:c.3254C>T XP_016864756.1:p.Pro1085Leu
XM_017009268.1:c.2945C>T XP_016864757.1:p.Pro982Leu
XR_001742050.2:n.3488C>T
XR_941095.1:n.3284C>T