Canonical Allele Identifier: CA448101408

Gene: FLT4

Linked Data

• dbSNP Id: rs1450801619
• gnomAD v3: 5-180610004-A-G
• gnomAD v4: 5-180610004-A-G
• MyVariant Identifiers: chr5:g.180037004A>G (hg19) ; chr5:g.180610004A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180610004A>G , CM000667.2:g.180610004A>G	GRCh38
NC_000005.9:g.180037004A>G , CM000667.1:g.180037004A>G	GRCh37
NC_000005.8:g.179969610A>G	NCBI36
NG_011536.1:g.44621T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3708T>C MANE Select	ENSP00000261937.6:p.Phe1236=
ENST00000261937.10:c.3708T>C	ENSP00000261937.6:p.Phe1236=
ENST00000393347.7:c.3708T>C	ENSP00000377016.3:p.Phe1236=
ENST00000502603.5:n.408T>C
ENST00000502649.5:c.3708T>C	ENSP00000426057.1:p.Phe1236=
ENST00000507059.5:n.4058T>C
ENST00000619105.4:c.*2651T>C	ENSP00000481134.1:n.*2651T>C
NM_002020.4:c.3708T>C	NP_002011.2:p.Phe1236=
NM_182925.4:c.3708T>C	NP_891555.2:p.Phe1236=
XM_011534477.1:c.3957T>C	XP_011532779.1:p.Phe1319=
XM_011534478.1:c.3939T>C	XP_011532780.1:p.Phe1313=
XM_011534479.1:c.3957T>C	XP_011532781.1:p.Phe1319=
XM_011534480.1:c.3957T>C	XP_011532782.1:p.Phe1319=
XM_011534481.1:c.3957T>C	XP_011532783.1:p.Phe1319=
XM_011534482.1:c.3726T>C	XP_011532784.1:p.Phe1242=
XM_011534483.1:c.3648T>C	XP_011532785.1:p.Phe1216=
XM_011534484.1:c.3249T>C	XP_011532786.1:p.Phe1083=
XR_941095.1:n.3994T>C
NM_001354989.1:c.3708T>C	NP_001341918.1:p.Phe1236=
XM_011534478.3:c.3939T>C	XP_011532780.1:p.Phe1313=
XM_011534484.2:c.3249T>C	XP_011532786.1:p.Phe1083=
XM_017009263.1:c.3939T>C	XP_016864752.1:p.Phe1313=
XM_017009264.2:c.3939T>C	XP_016864753.1:p.Phe1313=
XM_017009265.1:c.3939T>C	XP_016864754.1:p.Phe1313=
XM_017009266.1:c.3939T>C	XP_016864755.1:p.Phe1313=
XM_017009267.2:c.3939T>C	XP_016864756.1:p.Phe1313=
XM_017009268.1:c.3630T>C	XP_016864757.1:p.Phe1210=
XR_001742050.2:n.4198T>C
NM_182925.5:c.3708T>C MANE Select	NP_891555.2:p.Phe1236=
NM_001354989.2:c.3708T>C	NP_001341918.1:p.Phe1236=
NM_002020.5:c.3708T>C	NP_002011.2:p.Phe1236=