Canonical Allele Identifier: CA362495953

Gene: FLT4

Linked Data

• dbSNP Id: rs1180832689
• gnomAD v2: 5-180030308-C-G
• gnomAD v4: 5-180603308-C-G
• MyVariant Identifiers: chr5:g.180030308C>G (hg19) ; chr5:g.180603308C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3976G>C MANE Select	ENSP00000261937.6:p.Ala1326Pro
ENST00000261937.10:c.3976G>C	ENSP00000261937.6:p.Ala1326Pro
ENST00000502603.5:n.676G>C
NM_182925.4:c.3976G>C	NP_891555.2:p.Ala1326Pro
XM_011534477.1:c.4225G>C	XP_011532779.1:p.Ala1409Pro
XM_011534478.1:c.4207G>C	XP_011532780.1:p.Ala1403Pro
XM_011534479.1:c.*122G>C	XP_011532781.1:n.*122G>C
XM_011534482.1:c.3994G>C	XP_011532784.1:p.Ala1332Pro
XM_011534483.1:c.3916G>C	XP_011532785.1:p.Ala1306Pro
XM_011534484.1:c.3517G>C	XP_011532786.1:p.Ala1173Pro
XR_941095.1:n.4262G>C
XM_011534478.3:c.4207G>C	XP_011532780.1:p.Ala1403Pro
XM_011534484.2:c.3517G>C	XP_011532786.1:p.Ala1173Pro
XM_017009263.1:c.*122G>C	XP_016864752.1:n.*122G>C
XM_017009268.1:c.3898G>C	XP_016864757.1:p.Ala1300Pro
XR_001742050.2:n.4466G>C
NM_182925.5:c.3976G>C MANE Select	NP_891555.2:p.Ala1326Pro