Canonical Allele Identifier: CA1604713953

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603310C= , CM000667.2:g.180603310C=	GRCh38
NC_000005.9:g.180030310C= , CM000667.1:g.180030310C=	GRCh37
NC_000005.8:g.179962916C=	NCBI36
NG_011536.1:g.51315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3974G= MANE Select	ENSP00000261937.6:p.Gly1325=
ENST00000261937.10:c.3974G=	ENSP00000261937.6:p.Gly1325=
ENST00000502603.5:n.674G=
NM_182925.4:c.3974G=	NP_891555.2:p.Gly1325=
XM_011534477.1:c.4223G=	XP_011532779.1:p.Gly1408=
XM_011534478.1:c.4205G=	XP_011532780.1:p.Gly1402=
XM_011534479.1:c.*120G=	XP_011532781.1:n.*120G=
XM_011534482.1:c.3992G=	XP_011532784.1:p.Gly1331=
XM_011534483.1:c.3914G=	XP_011532785.1:p.Gly1305=
XM_011534484.1:c.3515G=	XP_011532786.1:p.Gly1172=
XR_941095.1:n.4260G=
XM_011534478.3:c.4205G=	XP_011532780.1:p.Gly1402=
XM_011534484.2:c.3515G=	XP_011532786.1:p.Gly1172=
XM_017009263.1:c.*120G=	XP_016864752.1:n.*120G=
XM_017009268.1:c.3896G=	XP_016864757.1:p.Gly1299=
XR_001742050.2:n.4464G=
NM_182925.5:c.3974G= MANE Select	NP_891555.2:p.Gly1325=