Canonical Allele Identifier: CA362496186

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030353C>G (hg19) ; chr5:g.180603353C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603353C>G , CM000667.2:g.180603353C>G	GRCh38
NC_000005.9:g.180030353C>G , CM000667.1:g.180030353C>G	GRCh37
NC_000005.8:g.179962959C>G	NCBI36
NG_011536.1:g.51272G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3931G>C MANE Select	ENSP00000261937.6:p.Ala1311Pro
ENST00000261937.10:c.3931G>C	ENSP00000261937.6:p.Ala1311Pro
ENST00000502603.5:n.631G>C
NM_182925.4:c.3931G>C	NP_891555.2:p.Ala1311Pro
XM_011534477.1:c.4180G>C	XP_011532779.1:p.Ala1394Pro
XM_011534478.1:c.4162G>C	XP_011532780.1:p.Ala1388Pro
XM_011534479.1:c.*77G>C	XP_011532781.1:n.*77G>C
XM_011534482.1:c.3949G>C	XP_011532784.1:p.Ala1317Pro
XM_011534483.1:c.3871G>C	XP_011532785.1:p.Ala1291Pro
XM_011534484.1:c.3472G>C	XP_011532786.1:p.Ala1158Pro
XR_941095.1:n.4217G>C
XM_011534478.3:c.4162G>C	XP_011532780.1:p.Ala1388Pro
XM_011534484.2:c.3472G>C	XP_011532786.1:p.Ala1158Pro
XM_017009263.1:c.*77G>C	XP_016864752.1:n.*77G>C
XM_017009268.1:c.3853G>C	XP_016864757.1:p.Ala1285Pro
XR_001742050.2:n.4421G>C
NM_182925.5:c.3931G>C MANE Select	NP_891555.2:p.Ala1311Pro