Canonical Allele Identifier: CA362495322

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030194A>C (hg19) ; chr5:g.180603194A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603194A>C , CM000667.2:g.180603194A>C	GRCh38
NC_000005.9:g.180030194A>C , CM000667.1:g.180030194A>C	GRCh37
NC_000005.8:g.179962800A>C	NCBI36
NG_011536.1:g.51431T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4090T>G MANE Select	ENSP00000261937.6:p.Ter1364Glu
ENST00000261937.10:c.4090T>G	ENSP00000261937.6:p.Ter1364Glu
ENST00000502603.5:n.790T>G
NM_182925.4:c.4090T>G	NP_891555.2:p.Ter1364Glu
XM_011534477.1:c.4339T>G	XP_011532779.1:p.Ter1447Glu
XM_011534478.1:c.4321T>G	XP_011532780.1:p.Ter1441Glu
XM_011534482.1:c.4108T>G	XP_011532784.1:p.Ter1370Glu
XM_011534483.1:c.4030T>G	XP_011532785.1:p.Ter1344Glu
XM_011534484.1:c.3631T>G	XP_011532786.1:p.Ter1211Glu
XR_941095.1:n.4376T>G
XM_011534478.3:c.4321T>G	XP_011532780.1:p.Ter1441Glu
XM_011534484.2:c.3631T>G	XP_011532786.1:p.Ter1211Glu
XM_017009263.1:c.*236T>G	XP_016864752.1:n.*236T>G
XM_017009268.1:c.4012T>G	XP_016864757.1:p.Ter1338Glu
XR_001742050.2:n.4580T>G
NM_182925.5:c.4090T>G MANE Select	NP_891555.2:p.Ter1364Glu