Canonical Allele Identifier: CA448098915

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030192T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603192T>C , CM000667.2:g.180603192T>C	GRCh38
NC_000005.9:g.180030192T>C , CM000667.1:g.180030192T>C	GRCh37
NC_000005.8:g.179962798T>C	NCBI36
NG_011536.1:g.51433A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4092A>G MANE Select	ENSP00000261937.6:p.Ter1364=
ENST00000261937.10:c.4092A>G	ENSP00000261937.6:p.Ter1364=
ENST00000502603.5:n.792A>G
NM_182925.4:c.4092A>G	NP_891555.2:p.Ter1364=
XM_011534477.1:c.4341A>G	XP_011532779.1:p.Ter1447=
XM_011534478.1:c.4323A>G	XP_011532780.1:p.Ter1441=
XM_011534482.1:c.4110A>G	XP_011532784.1:p.Ter1370=
XM_011534483.1:c.4032A>G	XP_011532785.1:p.Ter1344=
XM_011534484.1:c.3633A>G	XP_011532786.1:p.Ter1211=
XR_941095.1:n.4378A>G
XM_011534478.3:c.4323A>G	XP_011532780.1:p.Ter1441=
XM_011534484.2:c.3633A>G	XP_011532786.1:p.Ter1211=
XM_017009263.1:c.*238A>G	XP_016864752.1:n.*238A>G
XM_017009268.1:c.4014A>G	XP_016864757.1:p.Ter1338=
XR_001742050.2:n.4582A>G
NM_182925.5:c.4092A>G MANE Select	NP_891555.2:p.Ter1364=