Canonical Allele Identifier: CA362496312

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030376C>A (hg19) ; chr5:g.180603376C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603376C>A , CM000667.2:g.180603376C>A	GRCh38
NC_000005.9:g.180030376C>A , CM000667.1:g.180030376C>A	GRCh37
NC_000005.8:g.179962982C>A	NCBI36
NG_011536.1:g.51249G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3908G>T MANE Select	ENSP00000261937.6:p.Gly1303Val
ENST00000261937.10:c.3908G>T	ENSP00000261937.6:p.Gly1303Val
ENST00000502603.5:n.608G>T
NM_182925.4:c.3908G>T	NP_891555.2:p.Gly1303Val
XM_011534477.1:c.4157G>T	XP_011532779.1:p.Gly1386Val
XM_011534478.1:c.4139G>T	XP_011532780.1:p.Gly1380Val
XM_011534479.1:c.*54G>T	XP_011532781.1:n.*54G>T
XM_011534482.1:c.3926G>T	XP_011532784.1:p.Gly1309Val
XM_011534483.1:c.3848G>T	XP_011532785.1:p.Gly1283Val
XM_011534484.1:c.3449G>T	XP_011532786.1:p.Gly1150Val
XR_941095.1:n.4194G>T
XM_011534478.3:c.4139G>T	XP_011532780.1:p.Gly1380Val
XM_011534484.2:c.3449G>T	XP_011532786.1:p.Gly1150Val
XM_017009263.1:c.*54G>T	XP_016864752.1:n.*54G>T
XM_017009268.1:c.3830G>T	XP_016864757.1:p.Gly1277Val
XR_001742050.2:n.4398G>T
NM_182925.5:c.3908G>T MANE Select	NP_891555.2:p.Gly1303Val