Canonical Allele Identifier: CA1604713887

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603197A= , CM000667.2:g.180603197A=	GRCh38
NC_000005.9:g.180030197A= , CM000667.1:g.180030197A=	GRCh37
NC_000005.8:g.179962803A=	NCBI36
NG_011536.1:g.51428T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4087T= MANE Select	ENSP00000261937.6:p.Tyr1363=
ENST00000261937.10:c.4087T=	ENSP00000261937.6:p.Tyr1363=
ENST00000502603.5:n.787T=
NM_182925.4:c.4087T=	NP_891555.2:p.Tyr1363=
XM_011534477.1:c.4336T=	XP_011532779.1:p.Tyr1446=
XM_011534478.1:c.4318T=	XP_011532780.1:p.Tyr1440=
XM_011534482.1:c.4105T=	XP_011532784.1:p.Tyr1369=
XM_011534483.1:c.4027T=	XP_011532785.1:p.Tyr1343=
XM_011534484.1:c.3628T=	XP_011532786.1:p.Tyr1210=
XR_941095.1:n.4373T=
XM_011534478.3:c.4318T=	XP_011532780.1:p.Tyr1440=
XM_011534484.2:c.3628T=	XP_011532786.1:p.Tyr1210=
XM_017009263.1:c.*233T=	XP_016864752.1:n.*233T=
XM_017009268.1:c.4009T=	XP_016864757.1:p.Tyr1337=
XR_001742050.2:n.4577T=
NM_182925.5:c.4087T= MANE Select	NP_891555.2:p.Tyr1363=