Canonical Allele Identifier: CA1604713905

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603229G= , CM000667.2:g.180603229G=	GRCh38
NC_000005.9:g.180030229G= , CM000667.1:g.180030229G=	GRCh37
NC_000005.8:g.179962835G=	NCBI36
NG_011536.1:g.51396C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4055C= MANE Select	ENSP00000261937.6:p.Ser1352=
ENST00000261937.10:c.4055C=	ENSP00000261937.6:p.Ser1352=
ENST00000502603.5:n.755C=
NM_182925.4:c.4055C=	NP_891555.2:p.Ser1352=
XM_011534477.1:c.4304C=	XP_011532779.1:p.Ser1435=
XM_011534478.1:c.4286C=	XP_011532780.1:p.Ser1429=
XM_011534482.1:c.4073C=	XP_011532784.1:p.Ser1358=
XM_011534483.1:c.3995C=	XP_011532785.1:p.Ser1332=
XM_011534484.1:c.3596C=	XP_011532786.1:p.Ser1199=
XR_941095.1:n.4341C=
XM_011534478.3:c.4286C=	XP_011532780.1:p.Ser1429=
XM_011534484.2:c.3596C=	XP_011532786.1:p.Ser1199=
XM_017009263.1:c.*201C=	XP_016864752.1:n.*201C=
XM_017009268.1:c.3977C=	XP_016864757.1:p.Ser1326=
XR_001742050.2:n.4545C=
NM_182925.5:c.4055C= MANE Select	NP_891555.2:p.Ser1352=