Canonical Allele Identifier: CA362495941

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603305-G-C
• MyVariant Identifiers: chr5:g.180030305G>C (hg19) ; chr5:g.180603305G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603305G>C , CM000667.2:g.180603305G>C	GRCh38
NC_000005.9:g.180030305G>C , CM000667.1:g.180030305G>C	GRCh37
NC_000005.8:g.179962911G>C	NCBI36
NG_011536.1:g.51320C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3979C>G MANE Select	ENSP00000261937.6:p.Arg1327Gly
ENST00000261937.10:c.3979C>G	ENSP00000261937.6:p.Arg1327Gly
ENST00000502603.5:n.679C>G
NM_182925.4:c.3979C>G	NP_891555.2:p.Arg1327Gly
XM_011534477.1:c.4228C>G	XP_011532779.1:p.Arg1410Gly
XM_011534478.1:c.4210C>G	XP_011532780.1:p.Arg1404Gly
XM_011534479.1:c.*125C>G	XP_011532781.1:n.*125C>G
XM_011534482.1:c.3997C>G	XP_011532784.1:p.Arg1333Gly
XM_011534483.1:c.3919C>G	XP_011532785.1:p.Arg1307Gly
XM_011534484.1:c.3520C>G	XP_011532786.1:p.Arg1174Gly
XR_941095.1:n.4265C>G
XM_011534478.3:c.4210C>G	XP_011532780.1:p.Arg1404Gly
XM_011534484.2:c.3520C>G	XP_011532786.1:p.Arg1174Gly
XM_017009263.1:c.*125C>G	XP_016864752.1:n.*125C>G
XM_017009268.1:c.3901C>G	XP_016864757.1:p.Arg1301Gly
XR_001742050.2:n.4469C>G
NM_182925.5:c.3979C>G MANE Select	NP_891555.2:p.Arg1327Gly