Canonical Allele Identifier: CA3606565

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180621641G>A , CM000667.2:g.180621641G>A	GRCh38
NC_000005.9:g.180048641G>A , CM000667.1:g.180048641G>A	GRCh37
NC_000005.8:g.179981247G>A	NCBI36
NG_011536.1:g.32984C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.1921C>T MANE Select	ENSP00000261937.6:p.Pro641Ser
ENST00000261937.10:c.1921C>T	ENSP00000261937.6:p.Pro641Ser
ENST00000393347.7:c.1921C>T	ENSP00000377016.3:p.Pro641Ser
ENST00000424276.6:n.1921C>T
ENST00000502649.5:c.1921C>T	ENSP00000426057.1:p.Pro641Ser
ENST00000507059.5:n.1016C>T
ENST00000619105.4:c.*864C>T	ENSP00000481134.1:n.*864C>T
NM_002020.4:c.1921C>T	NP_002011.2:p.Pro641Ser
NM_182925.4:c.1921C>T	NP_891555.2:p.Pro641Ser
XM_011534477.1:c.2170C>T	XP_011532779.1:p.Pro724Ser
XM_011534478.1:c.2152C>T	XP_011532780.1:p.Pro718Ser
XM_011534479.1:c.2170C>T	XP_011532781.1:p.Pro724Ser
XM_011534480.1:c.2170C>T	XP_011532782.1:p.Pro724Ser
XM_011534481.1:c.2170C>T	XP_011532783.1:p.Pro724Ser
XM_011534482.1:c.1939C>T	XP_011532784.1:p.Pro647Ser
XM_011534483.1:c.1861C>T	XP_011532785.1:p.Pro621Ser
XM_011534484.1:c.1462C>T	XP_011532786.1:p.Pro488Ser
XR_941095.1:n.2182C>T
NM_001354989.1:c.1921C>T	NP_001341918.1:p.Pro641Ser
XM_011534478.3:c.2152C>T	XP_011532780.1:p.Pro718Ser
XM_011534484.2:c.1462C>T	XP_011532786.1:p.Pro488Ser
XM_017009263.1:c.2152C>T	XP_016864752.1:p.Pro718Ser
XM_017009264.2:c.2152C>T	XP_016864753.1:p.Pro718Ser
XM_017009265.1:c.2152C>T	XP_016864754.1:p.Pro718Ser
XM_017009266.1:c.2152C>T	XP_016864755.1:p.Pro718Ser
XM_017009267.2:c.2152C>T	XP_016864756.1:p.Pro718Ser
XM_017009268.1:c.1843C>T	XP_016864757.1:p.Pro615Ser
XR_001742050.2:n.2386C>T
NM_182925.5:c.1921C>T MANE Select	NP_891555.2:p.Pro641Ser
NM_001354989.2:c.1921C>T	NP_001341918.1:p.Pro641Ser
NM_002020.5:c.1921C>T	NP_002011.2:p.Pro641Ser