Canonical Allele Identifier: CA362495933

Gene: FLT4

Linked Data

• dbSNP Id: rs747528649
• gnomAD v2: 5-180030304-C-A
• MyVariant Identifiers: chr5:g.180030304C>A (hg19) ; chr5:g.180603304C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603304C>A , CM000667.2:g.180603304C>A	GRCh38
NC_000005.9:g.180030304C>A , CM000667.1:g.180030304C>A	GRCh37
NC_000005.8:g.179962910C>A	NCBI36
NG_011536.1:g.51321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3980G>T MANE Select	ENSP00000261937.6:p.Arg1327Leu
ENST00000261937.10:c.3980G>T	ENSP00000261937.6:p.Arg1327Leu
ENST00000502603.5:n.680G>T
NM_182925.4:c.3980G>T	NP_891555.2:p.Arg1327Leu
XM_011534477.1:c.4229G>T	XP_011532779.1:p.Arg1410Leu
XM_011534478.1:c.4211G>T	XP_011532780.1:p.Arg1404Leu
XM_011534479.1:c.*126G>T	XP_011532781.1:n.*126G>T
XM_011534482.1:c.3998G>T	XP_011532784.1:p.Arg1333Leu
XM_011534483.1:c.3920G>T	XP_011532785.1:p.Arg1307Leu
XM_011534484.1:c.3521G>T	XP_011532786.1:p.Arg1174Leu
XR_941095.1:n.4266G>T
XM_011534478.3:c.4211G>T	XP_011532780.1:p.Arg1404Leu
XM_011534484.2:c.3521G>T	XP_011532786.1:p.Arg1174Leu
XM_017009263.1:c.*126G>T	XP_016864752.1:n.*126G>T
XM_017009268.1:c.3902G>T	XP_016864757.1:p.Arg1301Leu
XR_001742050.2:n.4470G>T
NM_182925.5:c.3980G>T MANE Select	NP_891555.2:p.Arg1327Leu