Canonical Allele Identifier: CA133193998

Gene: FLT4

Linked Data

• dbSNP Id: rs1021827251
• gnomAD v4: 5-180603288-A-G
• MyVariant Identifiers: chr5:g.180030288A>G (hg19) ; chr5:g.180603288A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603288A>G , CM000667.2:g.180603288A>G	GRCh38
NC_000005.9:g.180030288A>G , CM000667.1:g.180030288A>G	GRCh37
NC_000005.8:g.179962894A>G	NCBI36
NG_011536.1:g.51337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3996T>C MANE Select	ENSP00000261937.6:p.Phe1332=
ENST00000261937.10:c.3996T>C	ENSP00000261937.6:p.Phe1332=
ENST00000502603.5:n.696T>C
NM_182925.4:c.3996T>C	NP_891555.2:p.Phe1332=
XM_011534477.1:c.4245T>C	XP_011532779.1:p.Phe1415=
XM_011534478.1:c.4227T>C	XP_011532780.1:p.Phe1409=
XM_011534482.1:c.4014T>C	XP_011532784.1:p.Phe1338=
XM_011534483.1:c.3936T>C	XP_011532785.1:p.Phe1312=
XM_011534484.1:c.3537T>C	XP_011532786.1:p.Phe1179=
XR_941095.1:n.4282T>C
XM_011534478.3:c.4227T>C	XP_011532780.1:p.Phe1409=
XM_011534484.2:c.3537T>C	XP_011532786.1:p.Phe1179=
XM_017009263.1:c.*142T>C	XP_016864752.1:n.*142T>C
XM_017009268.1:c.3918T>C	XP_016864757.1:p.Phe1306=
XR_001742050.2:n.4486T>C
NM_182925.5:c.3996T>C MANE Select	NP_891555.2:p.Phe1332=