Canonical Allele Identifier: CA448099040

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030270C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603270C>A , CM000667.2:g.180603270C>A	GRCh38
NC_000005.9:g.180030270C>A , CM000667.1:g.180030270C>A	GRCh37
NC_000005.8:g.179962876C>A	NCBI36
NG_011536.1:g.51355G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4014G>T MANE Select	ENSP00000261937.6:p.Gly1338=
ENST00000261937.10:c.4014G>T	ENSP00000261937.6:p.Gly1338=
ENST00000502603.5:n.714G>T
NM_182925.4:c.4014G>T	NP_891555.2:p.Gly1338=
XM_011534477.1:c.4263G>T	XP_011532779.1:p.Gly1421=
XM_011534478.1:c.4245G>T	XP_011532780.1:p.Gly1415=
XM_011534482.1:c.4032G>T	XP_011532784.1:p.Gly1344=
XM_011534483.1:c.3954G>T	XP_011532785.1:p.Gly1318=
XM_011534484.1:c.3555G>T	XP_011532786.1:p.Gly1185=
XR_941095.1:n.4300G>T
XM_011534478.3:c.4245G>T	XP_011532780.1:p.Gly1415=
XM_011534484.2:c.3555G>T	XP_011532786.1:p.Gly1185=
XM_017009263.1:c.*160G>T	XP_016864752.1:n.*160G>T
XM_017009268.1:c.3936G>T	XP_016864757.1:p.Gly1312=
XR_001742050.2:n.4504G>T
NM_182925.5:c.4014G>T MANE Select	NP_891555.2:p.Gly1338=