Canonical Allele Identifier: CA448099068

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030312C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603312C>G , CM000667.2:g.180603312C>G	GRCh38
NC_000005.9:g.180030312C>G , CM000667.1:g.180030312C>G	GRCh37
NC_000005.8:g.179962918C>G	NCBI36
NG_011536.1:g.51313G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3972G>C MANE Select	ENSP00000261937.6:p.Arg1324=
ENST00000261937.10:c.3972G>C	ENSP00000261937.6:p.Arg1324=
ENST00000502603.5:n.672G>C
NM_182925.4:c.3972G>C	NP_891555.2:p.Arg1324=
XM_011534477.1:c.4221G>C	XP_011532779.1:p.Arg1407=
XM_011534478.1:c.4203G>C	XP_011532780.1:p.Arg1401=
XM_011534479.1:c.*118G>C	XP_011532781.1:n.*118G>C
XM_011534482.1:c.3990G>C	XP_011532784.1:p.Arg1330=
XM_011534483.1:c.3912G>C	XP_011532785.1:p.Arg1304=
XM_011534484.1:c.3513G>C	XP_011532786.1:p.Arg1171=
XR_941095.1:n.4258G>C
XM_011534478.3:c.4203G>C	XP_011532780.1:p.Arg1401=
XM_011534484.2:c.3513G>C	XP_011532786.1:p.Arg1171=
XM_017009263.1:c.*118G>C	XP_016864752.1:n.*118G>C
XM_017009268.1:c.3894G>C	XP_016864757.1:p.Arg1298=
XR_001742050.2:n.4462G>C
NM_182925.5:c.3972G>C MANE Select	NP_891555.2:p.Arg1324=