Canonical Allele Identifier: CA448099121

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603375-G-T
• MyVariant Identifiers: chr5:g.180030375G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603375G>T , CM000667.2:g.180603375G>T	GRCh38
NC_000005.9:g.180030375G>T , CM000667.1:g.180030375G>T	GRCh37
NC_000005.8:g.179962981G>T	NCBI36
NG_011536.1:g.51250C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3909C>A MANE Select	ENSP00000261937.6:p.Gly1303=
ENST00000261937.10:c.3909C>A	ENSP00000261937.6:p.Gly1303=
ENST00000502603.5:n.609C>A
NM_182925.4:c.3909C>A	NP_891555.2:p.Gly1303=
XM_011534477.1:c.4158C>A	XP_011532779.1:p.Gly1386=
XM_011534478.1:c.4140C>A	XP_011532780.1:p.Gly1380=
XM_011534479.1:c.*55C>A	XP_011532781.1:n.*55C>A
XM_011534482.1:c.3927C>A	XP_011532784.1:p.Gly1309=
XM_011534483.1:c.3849C>A	XP_011532785.1:p.Gly1283=
XM_011534484.1:c.3450C>A	XP_011532786.1:p.Gly1150=
XR_941095.1:n.4195C>A
XM_011534478.3:c.4140C>A	XP_011532780.1:p.Gly1380=
XM_011534484.2:c.3450C>A	XP_011532786.1:p.Gly1150=
XM_017009263.1:c.*55C>A	XP_016864752.1:n.*55C>A
XM_017009268.1:c.3831C>A	XP_016864757.1:p.Gly1277=
XR_001742050.2:n.4399C>A
NM_182925.5:c.3909C>A MANE Select	NP_891555.2:p.Gly1303=