Canonical Allele Identifier: CA2769679490

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619501_180619502del , CM000667.2:g.180619501_180619502del	GRCh38
NC_000005.9:g.180046501_180046502del , CM000667.1:g.180046501_180046502del	GRCh37
NC_000005.8:g.179979107_179979108del	NCBI36
NG_011536.1:g.35123_35124del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-136_2648-135del MANE Select	ENSP00000261937.6:n.2648-136_2648-135del
ENST00000261937.10:c.2648-136_2648-135del	ENSP00000261937.6:n.2648-136_2648-135del
ENST00000393347.7:c.2648-136_2648-135del	ENSP00000377016.3:n.2648-136_2648-135del
ENST00000502649.5:c.2648-136_2648-135del	ENSP00000426057.1:n.2648-136_2648-135del
ENST00000507059.5:n.1905_1906del
ENST00000619105.4:c.*1591-136_*1591-135del	ENSP00000481134.1:n.*1591-136_*1591-135del
NM_002020.4:c.2648-136_2648-135del	NP_002011.2:n.2648-136_2648-135del
NM_182925.4:c.2648-136_2648-135del	NP_891555.2:n.2648-136_2648-135del
XM_011534477.1:c.2897-136_2897-135del	XP_011532779.1:n.2897-136_2897-135del
XM_011534478.1:c.2879-136_2879-135del	XP_011532780.1:n.2879-136_2879-135del
XM_011534479.1:c.2897-136_2897-135del	XP_011532781.1:n.2897-136_2897-135del
XM_011534480.1:c.2897-136_2897-135del	XP_011532782.1:n.2897-136_2897-135del
XM_011534481.1:c.2897-136_2897-135del	XP_011532783.1:n.2897-136_2897-135del
XM_011534482.1:c.2666-136_2666-135del	XP_011532784.1:n.2666-136_2666-135del
XM_011534483.1:c.2588-136_2588-135del	XP_011532785.1:n.2588-136_2588-135del
XM_011534484.1:c.2189-136_2189-135del	XP_011532786.1:n.2189-136_2189-135del
XR_941095.1:n.2909-136_2909-135del
NM_001354989.1:c.2648-136_2648-135del	NP_001341918.1:n.2648-136_2648-135del
XM_011534478.3:c.2879-136_2879-135del	XP_011532780.1:n.2879-136_2879-135del
XM_011534484.2:c.2189-136_2189-135del	XP_011532786.1:n.2189-136_2189-135del
XM_017009263.1:c.2879-136_2879-135del	XP_016864752.1:n.2879-136_2879-135del
XM_017009264.2:c.2879-136_2879-135del	XP_016864753.1:n.2879-136_2879-135del
XM_017009265.1:c.2879-136_2879-135del	XP_016864754.1:n.2879-136_2879-135del
XM_017009266.1:c.2879-136_2879-135del	XP_016864755.1:n.2879-136_2879-135del
XM_017009267.2:c.2879-136_2879-135del	XP_016864756.1:n.2879-136_2879-135del
XM_017009268.1:c.2570-136_2570-135del	XP_016864757.1:n.2570-136_2570-135del
XR_001742050.2:n.3113-136_3113-135del
NM_182925.5:c.2648-136_2648-135del MANE Select	NP_891555.2:n.2648-136_2648-135del
NM_001354989.2:c.2648-136_2648-135del	NP_001341918.1:n.2648-136_2648-135del
NM_002020.5:c.2648-136_2648-135del	NP_002011.2:n.2648-136_2648-135del