Canonical Allele Identifier: CA1604713947

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603299C= , CM000667.2:g.180603299C=	GRCh38
NC_000005.9:g.180030299C= , CM000667.1:g.180030299C=	GRCh37
NC_000005.8:g.179962905C=	NCBI36
NG_011536.1:g.51326G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3985G= MANE Select	ENSP00000261937.6:p.Gly1329=
ENST00000261937.10:c.3985G=	ENSP00000261937.6:p.Gly1329=
ENST00000502603.5:n.685G=
NM_182925.4:c.3985G=	NP_891555.2:p.Gly1329=
XM_011534477.1:c.4234G=	XP_011532779.1:p.Gly1412=
XM_011534478.1:c.4216G=	XP_011532780.1:p.Gly1406=
XM_011534482.1:c.4003G=	XP_011532784.1:p.Gly1335=
XM_011534483.1:c.3925G=	XP_011532785.1:p.Gly1309=
XM_011534484.1:c.3526G=	XP_011532786.1:p.Gly1176=
XR_941095.1:n.4271G=
XM_011534478.3:c.4216G=	XP_011532780.1:p.Gly1406=
XM_011534484.2:c.3526G=	XP_011532786.1:p.Gly1176=
XM_017009263.1:c.*131G=	XP_016864752.1:n.*131G=
XM_017009268.1:c.3907G=	XP_016864757.1:p.Gly1303=
XR_001742050.2:n.4475G=
NM_182925.5:c.3985G= MANE Select	NP_891555.2:p.Gly1329=