Canonical Allele Identifier: CA1604722897

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619425_180619426delinsAC , CM000667.2:g.180619425_180619426delinsAC	GRCh38
NC_000005.9:g.180046425_180046426delinsAC , CM000667.1:g.180046425_180046426delinsAC	GRCh37
NC_000005.8:g.179979031_179979032delinsAC	NCBI36
NG_011536.1:g.35199_35200delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-60_2648-59delinsGT MANE Select	ENSP00000261937.6:n.2648-60_2648-59delinsGT
ENST00000261937.10:c.2648-60_2648-59delinsGT	ENSP00000261937.6:n.2648-60_2648-59delinsGT
ENST00000393347.7:c.2648-60_2648-59delinsGT	ENSP00000377016.3:n.2648-60_2648-59delinsGT
ENST00000502649.5:c.2648-60_2648-59delinsGT	ENSP00000426057.1:n.2648-60_2648-59delinsGT
ENST00000507059.5:n.1981_1982delinsGT
ENST00000619105.4:c.*1591-60_*1591-59delinsGT	ENSP00000481134.1:n.*1591-60_*1591-59delinsGT
NM_002020.4:c.2648-60_2648-59delinsGT	NP_002011.2:n.2648-60_2648-59delinsGT
NM_182925.4:c.2648-60_2648-59delinsGT	NP_891555.2:n.2648-60_2648-59delinsGT
XM_011534477.1:c.2897-60_2897-59delinsGT	XP_011532779.1:n.2897-60_2897-59delinsGT
XM_011534478.1:c.2879-60_2879-59delinsGT	XP_011532780.1:n.2879-60_2879-59delinsGT
XM_011534479.1:c.2897-60_2897-59delinsGT	XP_011532781.1:n.2897-60_2897-59delinsGT
XM_011534480.1:c.2897-60_2897-59delinsGT	XP_011532782.1:n.2897-60_2897-59delinsGT
XM_011534481.1:c.2897-60_2897-59delinsGT	XP_011532783.1:n.2897-60_2897-59delinsGT
XM_011534482.1:c.2666-60_2666-59delinsGT	XP_011532784.1:n.2666-60_2666-59delinsGT
XM_011534483.1:c.2588-60_2588-59delinsGT	XP_011532785.1:n.2588-60_2588-59delinsGT
XM_011534484.1:c.2189-60_2189-59delinsGT	XP_011532786.1:n.2189-60_2189-59delinsGT
XR_941095.1:n.2909-60_2909-59delinsGT
NM_001354989.1:c.2648-60_2648-59delinsGT	NP_001341918.1:n.2648-60_2648-59delinsGT
XM_011534478.3:c.2879-60_2879-59delinsGT	XP_011532780.1:n.2879-60_2879-59delinsGT
XM_011534484.2:c.2189-60_2189-59delinsGT	XP_011532786.1:n.2189-60_2189-59delinsGT
XM_017009263.1:c.2879-60_2879-59delinsGT	XP_016864752.1:n.2879-60_2879-59delinsGT
XM_017009264.2:c.2879-60_2879-59delinsGT	XP_016864753.1:n.2879-60_2879-59delinsGT
XM_017009265.1:c.2879-60_2879-59delinsGT	XP_016864754.1:n.2879-60_2879-59delinsGT
XM_017009266.1:c.2879-60_2879-59delinsGT	XP_016864755.1:n.2879-60_2879-59delinsGT
XM_017009267.2:c.2879-60_2879-59delinsGT	XP_016864756.1:n.2879-60_2879-59delinsGT
XM_017009268.1:c.2570-60_2570-59delinsGT	XP_016864757.1:n.2570-60_2570-59delinsGT
XR_001742050.2:n.3113-60_3113-59delinsGT
NM_182925.5:c.2648-60_2648-59delinsGT MANE Select	NP_891555.2:n.2648-60_2648-59delinsGT
NM_001354989.2:c.2648-60_2648-59delinsGT	NP_001341918.1:n.2648-60_2648-59delinsGT
NM_002020.5:c.2648-60_2648-59delinsGT	NP_002011.2:n.2648-60_2648-59delinsGT