Canonical Allele Identifier: CA362495955

Gene: FLT4

Linked Data

• dbSNP Id: rs1180832689
• gnomAD v4: 5-180603308-C-T
• MyVariant Identifiers: chr5:g.180030308C>T (hg19) ; chr5:g.180603308C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603308C>T , CM000667.2:g.180603308C>T	GRCh38
NC_000005.9:g.180030308C>T , CM000667.1:g.180030308C>T	GRCh37
NC_000005.8:g.179962914C>T	NCBI36
NG_011536.1:g.51317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3976G>A MANE Select	ENSP00000261937.6:p.Ala1326Thr
ENST00000261937.10:c.3976G>A	ENSP00000261937.6:p.Ala1326Thr
ENST00000502603.5:n.676G>A
NM_182925.4:c.3976G>A	NP_891555.2:p.Ala1326Thr
XM_011534477.1:c.4225G>A	XP_011532779.1:p.Ala1409Thr
XM_011534478.1:c.4207G>A	XP_011532780.1:p.Ala1403Thr
XM_011534479.1:c.*122G>A	XP_011532781.1:n.*122G>A
XM_011534482.1:c.3994G>A	XP_011532784.1:p.Ala1332Thr
XM_011534483.1:c.3916G>A	XP_011532785.1:p.Ala1306Thr
XM_011534484.1:c.3517G>A	XP_011532786.1:p.Ala1173Thr
XR_941095.1:n.4262G>A
XM_011534478.3:c.4207G>A	XP_011532780.1:p.Ala1403Thr
XM_011534484.2:c.3517G>A	XP_011532786.1:p.Ala1173Thr
XM_017009263.1:c.*122G>A	XP_016864752.1:n.*122G>A
XM_017009268.1:c.3898G>A	XP_016864757.1:p.Ala1300Thr
XR_001742050.2:n.4466G>A
NM_182925.5:c.3976G>A MANE Select	NP_891555.2:p.Ala1326Thr