Canonical Allele Identifier: CA362495406

Gene: FLT4

Linked Data

• dbSNP Id: rs143739828
• MyVariant Identifiers: chr5:g.180030221C>G (hg19) ; chr5:g.180603221C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603221C>G , CM000667.2:g.180603221C>G	GRCh38
NC_000005.9:g.180030221C>G , CM000667.1:g.180030221C>G	GRCh37
NC_000005.8:g.179962827C>G	NCBI36
NG_011536.1:g.51404G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4063G>C MANE Select	ENSP00000261937.6:p.Val1355Leu
ENST00000261937.10:c.4063G>C	ENSP00000261937.6:p.Val1355Leu
ENST00000502603.5:n.763G>C
NM_182925.4:c.4063G>C	NP_891555.2:p.Val1355Leu
XM_011534477.1:c.4312G>C	XP_011532779.1:p.Val1438Leu
XM_011534478.1:c.4294G>C	XP_011532780.1:p.Val1432Leu
XM_011534482.1:c.4081G>C	XP_011532784.1:p.Val1361Leu
XM_011534483.1:c.4003G>C	XP_011532785.1:p.Val1335Leu
XM_011534484.1:c.3604G>C	XP_011532786.1:p.Val1202Leu
XR_941095.1:n.4349G>C
XM_011534478.3:c.4294G>C	XP_011532780.1:p.Val1432Leu
XM_011534484.2:c.3604G>C	XP_011532786.1:p.Val1202Leu
XM_017009263.1:c.*209G>C	XP_016864752.1:n.*209G>C
XM_017009268.1:c.3985G>C	XP_016864757.1:p.Val1329Leu
XR_001742050.2:n.4553G>C
NM_182925.5:c.4063G>C MANE Select	NP_891555.2:p.Val1355Leu