Canonical Allele Identifier: CA362495632

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030262G>C (hg19) ; chr5:g.180603262G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603262G>C , CM000667.2:g.180603262G>C	GRCh38
NC_000005.9:g.180030262G>C , CM000667.1:g.180030262G>C	GRCh37
NC_000005.8:g.179962868G>C	NCBI36
NG_011536.1:g.51363C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4022C>G MANE Select	ENSP00000261937.6:p.Ser1341Trp
ENST00000261937.10:c.4022C>G	ENSP00000261937.6:p.Ser1341Trp
ENST00000502603.5:n.722C>G
NM_182925.4:c.4022C>G	NP_891555.2:p.Ser1341Trp
XM_011534477.1:c.4271C>G	XP_011532779.1:p.Ser1424Trp
XM_011534478.1:c.4253C>G	XP_011532780.1:p.Ser1418Trp
XM_011534482.1:c.4040C>G	XP_011532784.1:p.Ser1347Trp
XM_011534483.1:c.3962C>G	XP_011532785.1:p.Ser1321Trp
XM_011534484.1:c.3563C>G	XP_011532786.1:p.Ser1188Trp
XR_941095.1:n.4308C>G
XM_011534478.3:c.4253C>G	XP_011532780.1:p.Ser1418Trp
XM_011534484.2:c.3563C>G	XP_011532786.1:p.Ser1188Trp
XM_017009263.1:c.*168C>G	XP_016864752.1:n.*168C>G
XM_017009268.1:c.3944C>G	XP_016864757.1:p.Ser1315Trp
XR_001742050.2:n.4512C>G
NM_182925.5:c.4022C>G MANE Select	NP_891555.2:p.Ser1341Trp