Canonical Allele Identifier: CA1604713969

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603346G= , CM000667.2:g.180603346G=	GRCh38
NC_000005.9:g.180030346G= , CM000667.1:g.180030346G=	GRCh37
NC_000005.8:g.179962952G=	NCBI36
NG_011536.1:g.51279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3938C= MANE Select	ENSP00000261937.6:p.Pro1313=
ENST00000261937.10:c.3938C=	ENSP00000261937.6:p.Pro1313=
ENST00000502603.5:n.638C=
NM_182925.4:c.3938C=	NP_891555.2:p.Pro1313=
XM_011534477.1:c.4187C=	XP_011532779.1:p.Pro1396=
XM_011534478.1:c.4169C=	XP_011532780.1:p.Pro1390=
XM_011534479.1:c.*84C=	XP_011532781.1:n.*84C=
XM_011534482.1:c.3956C=	XP_011532784.1:p.Pro1319=
XM_011534483.1:c.3878C=	XP_011532785.1:p.Pro1293=
XM_011534484.1:c.3479C=	XP_011532786.1:p.Pro1160=
XR_941095.1:n.4224C=
XM_011534478.3:c.4169C=	XP_011532780.1:p.Pro1390=
XM_011534484.2:c.3479C=	XP_011532786.1:p.Pro1160=
XM_017009263.1:c.*84C=	XP_016864752.1:n.*84C=
XM_017009268.1:c.3860C=	XP_016864757.1:p.Pro1287=
XR_001742050.2:n.4428C=
NM_182925.5:c.3938C= MANE Select	NP_891555.2:p.Pro1313=