Canonical Allele Identifier: CA133199278

Gene: FLT4

Linked Data

• dbSNP Id: rs986596464
• MyVariant Identifiers: chr5:g.180036797_180036798del (hg19) ; chr5:g.180609797_180609798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609798_180609799del , CM000667.2:g.180609798_180609799del	GRCh38
NC_000005.9:g.180036798_180036799del , CM000667.1:g.180036798_180036799del	GRCh37
NC_000005.8:g.179969404_179969405del	NCBI36
NG_011536.1:g.44827_44828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+107_3807+108del MANE Select	ENSP00000261937.6:n.3807+107_3807+108del
ENST00000261937.10:c.3807+107_3807+108del	ENSP00000261937.6:n.3807+107_3807+108del
ENST00000393347.7:c.3807+107_3807+108del	ENSP00000377016.3:n.3807+107_3807+108del
ENST00000502603.5:n.507+107_507+108del
ENST00000502649.5:c.3807+107_3807+108del	ENSP00000426057.1:n.3807+107_3807+108del
ENST00000507059.5:n.4264_4265del
ENST00000619105.4:c.*2750+107_*2750+108del	ENSP00000481134.1:n.*2750+107_*2750+108del
NM_002020.4:c.3807+107_3807+108del	NP_002011.2:n.3807+107_3807+108del
NM_182925.4:c.3807+107_3807+108del	NP_891555.2:n.3807+107_3807+108del
XM_011534477.1:c.4056+107_4056+108del	XP_011532779.1:n.4056+107_4056+108del
XM_011534478.1:c.4038+107_4038+108del	XP_011532780.1:n.4038+107_4038+108del
XM_011534479.1:c.4056+107_4056+108del	XP_011532781.1:n.4056+107_4056+108del
XM_011534480.1:c.4056+107_4056+108del	XP_011532782.1:n.4056+107_4056+108del
XM_011534481.1:c.4056+107_4056+108del	XP_011532783.1:n.4056+107_4056+108del
XM_011534482.1:c.3825+107_3825+108del	XP_011532784.1:n.3825+107_3825+108del
XM_011534483.1:c.3747+107_3747+108del	XP_011532785.1:n.3747+107_3747+108del
XM_011534484.1:c.3348+107_3348+108del	XP_011532786.1:n.3348+107_3348+108del
XR_941095.1:n.4093+107_4093+108del
NM_001354989.1:c.3807+107_3807+108del	NP_001341918.1:n.3807+107_3807+108del
XM_011534478.3:c.4038+107_4038+108del	XP_011532780.1:n.4038+107_4038+108del
XM_011534484.2:c.3348+107_3348+108del	XP_011532786.1:n.3348+107_3348+108del
XM_017009263.1:c.4038+107_4038+108del	XP_016864752.1:n.4038+107_4038+108del
XM_017009264.2:c.4038+107_4038+108del	XP_016864753.1:n.4038+107_4038+108del
XM_017009265.1:c.4038+107_4038+108del	XP_016864754.1:n.4038+107_4038+108del
XM_017009266.1:c.4038+107_4038+108del	XP_016864755.1:n.4038+107_4038+108del
XM_017009267.2:c.4038+107_4038+108del	XP_016864756.1:n.4038+107_4038+108del
XM_017009268.1:c.3729+107_3729+108del	XP_016864757.1:n.3729+107_3729+108del
XR_001742050.2:n.4297+107_4297+108del
NM_182925.5:c.3807+107_3807+108del MANE Select	NP_891555.2:n.3807+107_3807+108del
NM_001354989.2:c.3807+107_3807+108del	NP_001341918.1:n.3807+107_3807+108del
NM_002020.5:c.3807+107_3807+108del	NP_002011.2:n.3807+107_3807+108del