Canonical Allele Identifier: CA1604713927

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603262G= , CM000667.2:g.180603262G=	GRCh38
NC_000005.9:g.180030262G= , CM000667.1:g.180030262G=	GRCh37
NC_000005.8:g.179962868G=	NCBI36
NG_011536.1:g.51363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4022C= MANE Select	ENSP00000261937.6:p.Ser1341=
ENST00000261937.10:c.4022C=	ENSP00000261937.6:p.Ser1341=
ENST00000502603.5:n.722C=
NM_182925.4:c.4022C=	NP_891555.2:p.Ser1341=
XM_011534477.1:c.4271C=	XP_011532779.1:p.Ser1424=
XM_011534478.1:c.4253C=	XP_011532780.1:p.Ser1418=
XM_011534482.1:c.4040C=	XP_011532784.1:p.Ser1347=
XM_011534483.1:c.3962C=	XP_011532785.1:p.Ser1321=
XM_011534484.1:c.3563C=	XP_011532786.1:p.Ser1188=
XR_941095.1:n.4308C=
XM_011534478.3:c.4253C=	XP_011532780.1:p.Ser1418=
XM_011534484.2:c.3563C=	XP_011532786.1:p.Ser1188=
XM_017009263.1:c.*168C=	XP_016864752.1:n.*168C=
XM_017009268.1:c.3944C=	XP_016864757.1:p.Ser1315=
XR_001742050.2:n.4512C=
NM_182925.5:c.4022C= MANE Select	NP_891555.2:p.Ser1341=