Canonical Allele Identifier: CA362496022

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030322C>G (hg19) ; chr5:g.180603322C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603322C>G , CM000667.2:g.180603322C>G	GRCh38
NC_000005.9:g.180030322C>G , CM000667.1:g.180030322C>G	GRCh37
NC_000005.8:g.179962928C>G	NCBI36
NG_011536.1:g.51303G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3962G>C MANE Select	ENSP00000261937.6:p.Arg1321Pro
ENST00000261937.10:c.3962G>C	ENSP00000261937.6:p.Arg1321Pro
ENST00000502603.5:n.662G>C
NM_182925.4:c.3962G>C	NP_891555.2:p.Arg1321Pro
XM_011534477.1:c.4211G>C	XP_011532779.1:p.Arg1404Pro
XM_011534478.1:c.4193G>C	XP_011532780.1:p.Arg1398Pro
XM_011534479.1:c.*108G>C	XP_011532781.1:n.*108G>C
XM_011534482.1:c.3980G>C	XP_011532784.1:p.Arg1327Pro
XM_011534483.1:c.3902G>C	XP_011532785.1:p.Arg1301Pro
XM_011534484.1:c.3503G>C	XP_011532786.1:p.Arg1168Pro
XR_941095.1:n.4248G>C
XM_011534478.3:c.4193G>C	XP_011532780.1:p.Arg1398Pro
XM_011534484.2:c.3503G>C	XP_011532786.1:p.Arg1168Pro
XM_017009263.1:c.*108G>C	XP_016864752.1:n.*108G>C
XM_017009268.1:c.3884G>C	XP_016864757.1:p.Arg1295Pro
XR_001742050.2:n.4452G>C
NM_182925.5:c.3962G>C MANE Select	NP_891555.2:p.Arg1321Pro