Canonical Allele Identifier: CA362495785

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603279-G-C
• MyVariant Identifiers: chr5:g.180030279G>C (hg19) ; chr5:g.180603279G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603279G>C , CM000667.2:g.180603279G>C	GRCh38
NC_000005.9:g.180030279G>C , CM000667.1:g.180030279G>C	GRCh37
NC_000005.8:g.179962885G>C	NCBI36
NG_011536.1:g.51346C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4005C>G MANE Select	ENSP00000261937.6:p.Ser1335Arg
ENST00000261937.10:c.4005C>G	ENSP00000261937.6:p.Ser1335Arg
ENST00000502603.5:n.705C>G
NM_182925.4:c.4005C>G	NP_891555.2:p.Ser1335Arg
XM_011534477.1:c.4254C>G	XP_011532779.1:p.Ser1418Arg
XM_011534478.1:c.4236C>G	XP_011532780.1:p.Ser1412Arg
XM_011534482.1:c.4023C>G	XP_011532784.1:p.Ser1341Arg
XM_011534483.1:c.3945C>G	XP_011532785.1:p.Ser1315Arg
XM_011534484.1:c.3546C>G	XP_011532786.1:p.Ser1182Arg
XR_941095.1:n.4291C>G
XM_011534478.3:c.4236C>G	XP_011532780.1:p.Ser1412Arg
XM_011534484.2:c.3546C>G	XP_011532786.1:p.Ser1182Arg
XM_017009263.1:c.*151C>G	XP_016864752.1:n.*151C>G
XM_017009268.1:c.3927C>G	XP_016864757.1:p.Ser1309Arg
XR_001742050.2:n.4495C>G
NM_182925.5:c.4005C>G MANE Select	NP_891555.2:p.Ser1335Arg