Canonical Allele Identifier: CA2695202870

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603273del , CM000667.2:g.180603273del	GRCh38
NC_000005.9:g.180030273del , CM000667.1:g.180030273del	GRCh37
NC_000005.8:g.179962879del	NCBI36
NG_011536.1:g.51352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4011del MANE Select	ENSP00000261937.6:p.Tyr1337Ter
ENST00000261937.10:c.4011del	ENSP00000261937.6:p.Tyr1337Ter
ENST00000502603.5:n.711del
NM_182925.4:c.4011del	NP_891555.2:p.Tyr1337Ter
XM_011534477.1:c.4260del	XP_011532779.1:p.Tyr1420Ter
XM_011534478.1:c.4242del	XP_011532780.1:p.Tyr1414Ter
XM_011534482.1:c.4029del	XP_011532784.1:p.Tyr1343Ter
XM_011534483.1:c.3951del	XP_011532785.1:p.Tyr1317Ter
XM_011534484.1:c.3552del	XP_011532786.1:p.Tyr1184Ter
XR_941095.1:n.4297del
XM_011534478.3:c.4242del	XP_011532780.1:p.Tyr1414Ter
XM_011534484.2:c.3552del	XP_011532786.1:p.Tyr1184Ter
XM_017009263.1:c.*157del	XP_016864752.1:n.*157del
XM_017009268.1:c.3933del	XP_016864757.1:p.Tyr1311Ter
XR_001742050.2:n.4501del
NM_182925.5:c.4011del MANE Select	NP_891555.2:p.Tyr1337Ter