Canonical Allele Identifier: CA1604713929

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603264C= , CM000667.2:g.180603264C=	GRCh38
NC_000005.9:g.180030264C= , CM000667.1:g.180030264C=	GRCh37
NC_000005.8:g.179962870C=	NCBI36
NG_011536.1:g.51361G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4020G= MANE Select	ENSP00000261937.6:p.Leu1340=
ENST00000261937.10:c.4020G=	ENSP00000261937.6:p.Leu1340=
ENST00000502603.5:n.720G=
NM_182925.4:c.4020G=	NP_891555.2:p.Leu1340=
XM_011534477.1:c.4269G=	XP_011532779.1:p.Leu1423=
XM_011534478.1:c.4251G=	XP_011532780.1:p.Leu1417=
XM_011534482.1:c.4038G=	XP_011532784.1:p.Leu1346=
XM_011534483.1:c.3960G=	XP_011532785.1:p.Leu1320=
XM_011534484.1:c.3561G=	XP_011532786.1:p.Leu1187=
XR_941095.1:n.4306G=
XM_011534478.3:c.4251G=	XP_011532780.1:p.Leu1417=
XM_011534484.2:c.3561G=	XP_011532786.1:p.Leu1187=
XM_017009263.1:c.*166G=	XP_016864752.1:n.*166G=
XM_017009268.1:c.3942G=	XP_016864757.1:p.Leu1314=
XR_001742050.2:n.4510G=
NM_182925.5:c.4020G= MANE Select	NP_891555.2:p.Leu1340=