Canonical Allele Identifier: CA1604713931

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603266G= , CM000667.2:g.180603266G=	GRCh38
NC_000005.9:g.180030266G= , CM000667.1:g.180030266G=	GRCh37
NC_000005.8:g.179962872G=	NCBI36
NG_011536.1:g.51359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4018C= MANE Select	ENSP00000261937.6:p.Leu1340=
ENST00000261937.10:c.4018C=	ENSP00000261937.6:p.Leu1340=
ENST00000502603.5:n.718C=
NM_182925.4:c.4018C=	NP_891555.2:p.Leu1340=
XM_011534477.1:c.4267C=	XP_011532779.1:p.Leu1423=
XM_011534478.1:c.4249C=	XP_011532780.1:p.Leu1417=
XM_011534482.1:c.4036C=	XP_011532784.1:p.Leu1346=
XM_011534483.1:c.3958C=	XP_011532785.1:p.Leu1320=
XM_011534484.1:c.3559C=	XP_011532786.1:p.Leu1187=
XR_941095.1:n.4304C=
XM_011534478.3:c.4249C=	XP_011532780.1:p.Leu1417=
XM_011534484.2:c.3559C=	XP_011532786.1:p.Leu1187=
XM_017009263.1:c.*164C=	XP_016864752.1:n.*164C=
XM_017009268.1:c.3940C=	XP_016864757.1:p.Leu1314=
XR_001742050.2:n.4508C=
NM_182925.5:c.4018C= MANE Select	NP_891555.2:p.Leu1340=