Canonical Allele Identifier: CA1604717455

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609920G= , CM000667.2:g.180609920G=	GRCh38
NC_000005.9:g.180036920G= , CM000667.1:g.180036920G=	GRCh37
NC_000005.8:g.179969526G=	NCBI36
NG_011536.1:g.44705C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3792C= MANE Select	ENSP00000261937.6:p.Thr1264=
ENST00000261937.10:c.3792C=	ENSP00000261937.6:p.Thr1264=
ENST00000393347.7:c.3792C=	ENSP00000377016.3:p.Thr1264=
ENST00000502603.5:n.492C=
ENST00000502649.5:c.3792C=	ENSP00000426057.1:p.Thr1264=
ENST00000507059.5:n.4142C=
ENST00000619105.4:c.*2735C=	ENSP00000481134.1:n.*2735C=
NM_002020.4:c.3792C=	NP_002011.2:p.Thr1264=
NM_182925.4:c.3792C=	NP_891555.2:p.Thr1264=
XM_011534477.1:c.4041C=	XP_011532779.1:p.Thr1347=
XM_011534478.1:c.4023C=	XP_011532780.1:p.Thr1341=
XM_011534479.1:c.4041C=	XP_011532781.1:p.Thr1347=
XM_011534480.1:c.4041C=	XP_011532782.1:p.Thr1347=
XM_011534481.1:c.4041C=	XP_011532783.1:p.Thr1347=
XM_011534482.1:c.3810C=	XP_011532784.1:p.Thr1270=
XM_011534483.1:c.3732C=	XP_011532785.1:p.Thr1244=
XM_011534484.1:c.3333C=	XP_011532786.1:p.Thr1111=
XR_941095.1:n.4078C=
NM_001354989.1:c.3792C=	NP_001341918.1:p.Thr1264=
XM_011534478.3:c.4023C=	XP_011532780.1:p.Thr1341=
XM_011534484.2:c.3333C=	XP_011532786.1:p.Thr1111=
XM_017009263.1:c.4023C=	XP_016864752.1:p.Thr1341=
XM_017009264.2:c.4023C=	XP_016864753.1:p.Thr1341=
XM_017009265.1:c.4023C=	XP_016864754.1:p.Thr1341=
XM_017009266.1:c.4023C=	XP_016864755.1:p.Thr1341=
XM_017009267.2:c.4023C=	XP_016864756.1:p.Thr1341=
XM_017009268.1:c.3714C=	XP_016864757.1:p.Thr1238=
XR_001742050.2:n.4282C=
NM_182925.5:c.3792C= MANE Select	NP_891555.2:p.Thr1264=
NM_001354989.2:c.3792C=	NP_001341918.1:p.Thr1264=
NM_002020.5:c.3792C=	NP_002011.2:p.Thr1264=