Canonical Allele Identifier: CA362500608

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180616477C>T , CM000667.2:g.180616477C>T	GRCh38
NC_000005.9:g.180043477C>T , CM000667.1:g.180043477C>T	GRCh37
NC_000005.8:g.179976083C>T	NCBI36
NG_011536.1:g.38148G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_182925.5:c.3109G>A MANE Select	NP_891555.2:p.Asp1037Asn
ENST00000261937.11:c.3109G>A MANE Select	ENSP00000261937.6:p.Asp1037Asn
NM_001354989.1:c.3109G>A	NP_001341918.1:p.Asp1037Asn
NM_001354989.2:c.3109G>A	NP_001341918.1:p.Asp1037Asn
NM_002020.4:c.3109G>A	NP_002011.2:p.Asp1037Asn
NM_002020.5:c.3109G>A	NP_002011.2:p.Asp1037Asn
NM_182925.4:c.3109G>A	NP_891555.2:p.Asp1037Asn
ENST00000261937.10:c.3109G>A	ENSP00000261937.6:p.Asp1037Asn
ENST00000393347.7:c.3109G>A	ENSP00000377016.3:p.Asp1037Asn
ENST00000502649.5:c.3109G>A	ENSP00000426057.1:p.Asp1037Asn
ENST00000507059.5:n.2502G>A
ENST00000512795.1:c.223G>A	ENSP00000421535.1:p.Asp75Asn
ENST00000514810.1:n.476G>A
ENST00000619105.4:c.*2052G>A	ENSP00000481134.1:n.*2052G>A
XM_011534477.1:c.3358G>A	XP_011532779.1:p.Asp1120Asn
XM_011534478.1:c.3340G>A	XP_011532780.1:p.Asp1114Asn
XM_011534478.3:c.3340G>A	XP_011532780.1:p.Asp1114Asn
XM_011534479.1:c.3358G>A	XP_011532781.1:p.Asp1120Asn
XM_011534480.1:c.3358G>A	XP_011532782.1:p.Asp1120Asn
XM_011534481.1:c.3358G>A	XP_011532783.1:p.Asp1120Asn
XM_011534482.1:c.3127G>A	XP_011532784.1:p.Asp1043Asn
XM_011534483.1:c.3049G>A	XP_011532785.1:p.Asp1017Asn
XM_011534484.1:c.2650G>A	XP_011532786.1:p.Asp884Asn
XM_011534484.2:c.2650G>A	XP_011532786.1:p.Asp884Asn
XM_017009263.1:c.3340G>A	XP_016864752.1:p.Asp1114Asn
XM_017009264.2:c.3340G>A	XP_016864753.1:p.Asp1114Asn
XM_017009265.1:c.3340G>A	XP_016864754.1:p.Asp1114Asn
XM_017009266.1:c.3340G>A	XP_016864755.1:p.Asp1114Asn
XM_017009267.2:c.3340G>A	XP_016864756.1:p.Asp1114Asn
XM_017009268.1:c.3031G>A	XP_016864757.1:p.Asp1011Asn
XR_001742050.2:n.3574G>A
XR_941095.1:n.3370G>A