Canonical Allele Identifier: CA1604713924

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603257G= , CM000667.2:g.180603257G=	GRCh38
NC_000005.9:g.180030257G= , CM000667.1:g.180030257G=	GRCh37
NC_000005.8:g.179962863G=	NCBI36
NG_011536.1:g.51368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4027C= MANE Select	ENSP00000261937.6:p.Pro1343=
ENST00000261937.10:c.4027C=	ENSP00000261937.6:p.Pro1343=
ENST00000502603.5:n.727C=
NM_182925.4:c.4027C=	NP_891555.2:p.Pro1343=
XM_011534477.1:c.4276C=	XP_011532779.1:p.Pro1426=
XM_011534478.1:c.4258C=	XP_011532780.1:p.Pro1420=
XM_011534482.1:c.4045C=	XP_011532784.1:p.Pro1349=
XM_011534483.1:c.3967C=	XP_011532785.1:p.Pro1323=
XM_011534484.1:c.3568C=	XP_011532786.1:p.Pro1190=
XR_941095.1:n.4313C=
XM_011534478.3:c.4258C=	XP_011532780.1:p.Pro1420=
XM_011534484.2:c.3568C=	XP_011532786.1:p.Pro1190=
XM_017009263.1:c.*173C=	XP_016864752.1:n.*173C=
XM_017009268.1:c.3949C=	XP_016864757.1:p.Pro1317=
XR_001742050.2:n.4517C=
NM_182925.5:c.4027C= MANE Select	NP_891555.2:p.Pro1343=