Canonical Allele Identifier: CA1604713917

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603244T= , CM000667.2:g.180603244T=	GRCh38
NC_000005.9:g.180030244T= , CM000667.1:g.180030244T=	GRCh37
NC_000005.8:g.179962850T=	NCBI36
NG_011536.1:g.51381A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4040A= MANE Select	ENSP00000261937.6:p.Asp1347=
ENST00000261937.10:c.4040A=	ENSP00000261937.6:p.Asp1347=
ENST00000502603.5:n.740A=
NM_182925.4:c.4040A=	NP_891555.2:p.Asp1347=
XM_011534477.1:c.4289A=	XP_011532779.1:p.Asp1430=
XM_011534478.1:c.4271A=	XP_011532780.1:p.Asp1424=
XM_011534482.1:c.4058A=	XP_011532784.1:p.Asp1353=
XM_011534483.1:c.3980A=	XP_011532785.1:p.Asp1327=
XM_011534484.1:c.3581A=	XP_011532786.1:p.Asp1194=
XR_941095.1:n.4326A=
XM_011534478.3:c.4271A=	XP_011532780.1:p.Asp1424=
XM_011534484.2:c.3581A=	XP_011532786.1:p.Asp1194=
XM_017009263.1:c.*186A=	XP_016864752.1:n.*186A=
XM_017009268.1:c.3962A=	XP_016864757.1:p.Asp1321=
XR_001742050.2:n.4530A=
NM_182925.5:c.4040A= MANE Select	NP_891555.2:p.Asp1347=