Canonical Allele Identifier: CA448098995

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030231C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603231C>G , CM000667.2:g.180603231C>G	GRCh38
NC_000005.9:g.180030231C>G , CM000667.1:g.180030231C>G	GRCh37
NC_000005.8:g.179962837C>G	NCBI36
NG_011536.1:g.51394G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4053G>C MANE Select	ENSP00000261937.6:p.Pro1351=
ENST00000261937.10:c.4053G>C	ENSP00000261937.6:p.Pro1351=
ENST00000502603.5:n.753G>C
NM_182925.4:c.4053G>C	NP_891555.2:p.Pro1351=
XM_011534477.1:c.4302G>C	XP_011532779.1:p.Pro1434=
XM_011534478.1:c.4284G>C	XP_011532780.1:p.Pro1428=
XM_011534482.1:c.4071G>C	XP_011532784.1:p.Pro1357=
XM_011534483.1:c.3993G>C	XP_011532785.1:p.Pro1331=
XM_011534484.1:c.3594G>C	XP_011532786.1:p.Pro1198=
XR_941095.1:n.4339G>C
XM_011534478.3:c.4284G>C	XP_011532780.1:p.Pro1428=
XM_011534484.2:c.3594G>C	XP_011532786.1:p.Pro1198=
XM_017009263.1:c.*199G>C	XP_016864752.1:n.*199G>C
XM_017009268.1:c.3975G>C	XP_016864757.1:p.Pro1325=
XR_001742050.2:n.4543G>C
NM_182925.5:c.4053G>C MANE Select	NP_891555.2:p.Pro1351=