Canonical Allele Identifier: CA362501880

Gene: FLT4

Linked Data

• gnomAD v4: 5-180619763-A-G
• MyVariant Identifiers: chr5:g.180046763A>G (hg19) ; chr5:g.180619763A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619763A>G , CM000667.2:g.180619763A>G	GRCh38
NC_000005.9:g.180046763A>G , CM000667.1:g.180046763A>G	GRCh37
NC_000005.8:g.179979369A>G	NCBI36
NG_011536.1:g.34862T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.2549T>C MANE Select	ENSP00000261937.6:p.Val850Ala
ENST00000261937.10:c.2549T>C	ENSP00000261937.6:p.Val850Ala
ENST00000393347.7:c.2549T>C	ENSP00000377016.3:p.Val850Ala
ENST00000502649.5:c.2549T>C	ENSP00000426057.1:p.Val850Ala
ENST00000507059.5:n.1644T>C
ENST00000619105.4:c.*1492T>C	ENSP00000481134.1:n.*1492T>C
NM_002020.4:c.2549T>C	NP_002011.2:p.Val850Ala
NM_182925.4:c.2549T>C	NP_891555.2:p.Val850Ala
XM_011534477.1:c.2798T>C	XP_011532779.1:p.Val933Ala
XM_011534478.1:c.2780T>C	XP_011532780.1:p.Val927Ala
XM_011534479.1:c.2798T>C	XP_011532781.1:p.Val933Ala
XM_011534480.1:c.2798T>C	XP_011532782.1:p.Val933Ala
XM_011534481.1:c.2798T>C	XP_011532783.1:p.Val933Ala
XM_011534482.1:c.2567T>C	XP_011532784.1:p.Val856Ala
XM_011534483.1:c.2489T>C	XP_011532785.1:p.Val830Ala
XM_011534484.1:c.2090T>C	XP_011532786.1:p.Val697Ala
XR_941095.1:n.2810T>C
NM_001354989.1:c.2549T>C	NP_001341918.1:p.Val850Ala
XM_011534478.3:c.2780T>C	XP_011532780.1:p.Val927Ala
XM_011534484.2:c.2090T>C	XP_011532786.1:p.Val697Ala
XM_017009263.1:c.2780T>C	XP_016864752.1:p.Val927Ala
XM_017009264.2:c.2780T>C	XP_016864753.1:p.Val927Ala
XM_017009265.1:c.2780T>C	XP_016864754.1:p.Val927Ala
XM_017009266.1:c.2780T>C	XP_016864755.1:p.Val927Ala
XM_017009267.2:c.2780T>C	XP_016864756.1:p.Val927Ala
XM_017009268.1:c.2471T>C	XP_016864757.1:p.Val824Ala
XR_001742050.2:n.3014T>C
NM_182925.5:c.2549T>C MANE Select	NP_891555.2:p.Val850Ala
NM_001354989.2:c.2549T>C	NP_001341918.1:p.Val850Ala
NM_002020.5:c.2549T>C	NP_002011.2:p.Val850Ala