Canonical Allele Identifier: CA362495597

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030257G>C (hg19) ; chr5:g.180603257G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603257G>C , CM000667.2:g.180603257G>C	GRCh38
NC_000005.9:g.180030257G>C , CM000667.1:g.180030257G>C	GRCh37
NC_000005.8:g.179962863G>C	NCBI36
NG_011536.1:g.51368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4027C>G MANE Select	ENSP00000261937.6:p.Pro1343Ala
ENST00000261937.10:c.4027C>G	ENSP00000261937.6:p.Pro1343Ala
ENST00000502603.5:n.727C>G
NM_182925.4:c.4027C>G	NP_891555.2:p.Pro1343Ala
XM_011534477.1:c.4276C>G	XP_011532779.1:p.Pro1426Ala
XM_011534478.1:c.4258C>G	XP_011532780.1:p.Pro1420Ala
XM_011534482.1:c.4045C>G	XP_011532784.1:p.Pro1349Ala
XM_011534483.1:c.3967C>G	XP_011532785.1:p.Pro1323Ala
XM_011534484.1:c.3568C>G	XP_011532786.1:p.Pro1190Ala
XR_941095.1:n.4313C>G
XM_011534478.3:c.4258C>G	XP_011532780.1:p.Pro1420Ala
XM_011534484.2:c.3568C>G	XP_011532786.1:p.Pro1190Ala
XM_017009263.1:c.*173C>G	XP_016864752.1:n.*173C>G
XM_017009268.1:c.3949C>G	XP_016864757.1:p.Pro1317Ala
XR_001742050.2:n.4517C>G
NM_182925.5:c.4027C>G MANE Select	NP_891555.2:p.Pro1343Ala