Canonical Allele Identifier: CA448098935

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030210G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603210G>A , CM000667.2:g.180603210G>A	GRCh38
NC_000005.9:g.180030210G>A , CM000667.1:g.180030210G>A	GRCh37
NC_000005.8:g.179962816G>A	NCBI36
NG_011536.1:g.51415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4074C>T MANE Select	ENSP00000261937.6:p.Phe1358=
ENST00000261937.10:c.4074C>T	ENSP00000261937.6:p.Phe1358=
ENST00000502603.5:n.774C>T
NM_182925.4:c.4074C>T	NP_891555.2:p.Phe1358=
XM_011534477.1:c.4323C>T	XP_011532779.1:p.Phe1441=
XM_011534478.1:c.4305C>T	XP_011532780.1:p.Phe1435=
XM_011534482.1:c.4092C>T	XP_011532784.1:p.Phe1364=
XM_011534483.1:c.4014C>T	XP_011532785.1:p.Phe1338=
XM_011534484.1:c.3615C>T	XP_011532786.1:p.Phe1205=
XR_941095.1:n.4360C>T
XM_011534478.3:c.4305C>T	XP_011532780.1:p.Phe1435=
XM_011534484.2:c.3615C>T	XP_011532786.1:p.Phe1205=
XM_017009263.1:c.*220C>T	XP_016864752.1:n.*220C>T
XM_017009268.1:c.3996C>T	XP_016864757.1:p.Phe1332=
XR_001742050.2:n.4564C>T
NM_182925.5:c.4074C>T MANE Select	NP_891555.2:p.Phe1358=