Canonical Allele Identifier: CA362495646

Gene: FLT4

Linked Data

• dbSNP Id: rs1458557842
• MyVariant Identifiers: chr5:g.180030263A>G (hg19) ; chr5:g.180603263A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603263A>G , CM000667.2:g.180603263A>G	GRCh38
NC_000005.9:g.180030263A>G , CM000667.1:g.180030263A>G	GRCh37
NC_000005.8:g.179962869A>G	NCBI36
NG_011536.1:g.51362T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4021T>C MANE Select	ENSP00000261937.6:p.Ser1341Pro
ENST00000261937.10:c.4021T>C	ENSP00000261937.6:p.Ser1341Pro
ENST00000502603.5:n.721T>C
NM_182925.4:c.4021T>C	NP_891555.2:p.Ser1341Pro
XM_011534477.1:c.4270T>C	XP_011532779.1:p.Ser1424Pro
XM_011534478.1:c.4252T>C	XP_011532780.1:p.Ser1418Pro
XM_011534482.1:c.4039T>C	XP_011532784.1:p.Ser1347Pro
XM_011534483.1:c.3961T>C	XP_011532785.1:p.Ser1321Pro
XM_011534484.1:c.3562T>C	XP_011532786.1:p.Ser1188Pro
XR_941095.1:n.4307T>C
XM_011534478.3:c.4252T>C	XP_011532780.1:p.Ser1418Pro
XM_011534484.2:c.3562T>C	XP_011532786.1:p.Ser1188Pro
XM_017009263.1:c.*167T>C	XP_016864752.1:n.*167T>C
XM_017009268.1:c.3943T>C	XP_016864757.1:p.Ser1315Pro
XR_001742050.2:n.4511T>C
NM_182925.5:c.4021T>C MANE Select	NP_891555.2:p.Ser1341Pro