Canonical Allele Identifier: CA1604713889

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603201G= , CM000667.2:g.180603201G=	GRCh38
NC_000005.9:g.180030201G= , CM000667.1:g.180030201G=	GRCh37
NC_000005.8:g.179962807G=	NCBI36
NG_011536.1:g.51424C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4083C= MANE Select	ENSP00000261937.6:p.Asn1361=
ENST00000261937.10:c.4083C=	ENSP00000261937.6:p.Asn1361=
ENST00000502603.5:n.783C=
NM_182925.4:c.4083C=	NP_891555.2:p.Asn1361=
XM_011534477.1:c.4332C=	XP_011532779.1:p.Asn1444=
XM_011534478.1:c.4314C=	XP_011532780.1:p.Asn1438=
XM_011534482.1:c.4101C=	XP_011532784.1:p.Asn1367=
XM_011534483.1:c.4023C=	XP_011532785.1:p.Asn1341=
XM_011534484.1:c.3624C=	XP_011532786.1:p.Asn1208=
XR_941095.1:n.4369C=
XM_011534478.3:c.4314C=	XP_011532780.1:p.Asn1438=
XM_011534484.2:c.3624C=	XP_011532786.1:p.Asn1208=
XM_017009263.1:c.*229C=	XP_016864752.1:n.*229C=
XM_017009268.1:c.4005C=	XP_016864757.1:p.Asn1335=
XR_001742050.2:n.4573C=
NM_182925.5:c.4083C= MANE Select	NP_891555.2:p.Asn1361=