Canonical Allele Identifier: CA362495398

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030220A>C (hg19) ; chr5:g.180603220A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603220A>C , CM000667.2:g.180603220A>C	GRCh38
NC_000005.9:g.180030220A>C , CM000667.1:g.180030220A>C	GRCh37
NC_000005.8:g.179962826A>C	NCBI36
NG_011536.1:g.51405T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4064T>G MANE Select	ENSP00000261937.6:p.Val1355Gly
ENST00000261937.10:c.4064T>G	ENSP00000261937.6:p.Val1355Gly
ENST00000502603.5:n.764T>G
NM_182925.4:c.4064T>G	NP_891555.2:p.Val1355Gly
XM_011534477.1:c.4313T>G	XP_011532779.1:p.Val1438Gly
XM_011534478.1:c.4295T>G	XP_011532780.1:p.Val1432Gly
XM_011534482.1:c.4082T>G	XP_011532784.1:p.Val1361Gly
XM_011534483.1:c.4004T>G	XP_011532785.1:p.Val1335Gly
XM_011534484.1:c.3605T>G	XP_011532786.1:p.Val1202Gly
XR_941095.1:n.4350T>G
XM_011534478.3:c.4295T>G	XP_011532780.1:p.Val1432Gly
XM_011534484.2:c.3605T>G	XP_011532786.1:p.Val1202Gly
XM_017009263.1:c.*210T>G	XP_016864752.1:n.*210T>G
XM_017009268.1:c.3986T>G	XP_016864757.1:p.Val1329Gly
XR_001742050.2:n.4554T>G
NM_182925.5:c.4064T>G MANE Select	NP_891555.2:p.Val1355Gly