Canonical Allele Identifier: CA126343

Gene: FLT4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180618911G>A , CM000667.2:g.180618911G>A	GRCh38
NC_000005.9:g.180045911G>A , CM000667.1:g.180045911G>A	GRCh37
NC_000005.8:g.179978517G>A	NCBI36
NG_011536.1:g.35714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2860C>T MANE Select	ENSP00000261937.6:p.Pro954Ser
ENST00000261937.10:c.2860C>T	ENSP00000261937.6:p.Pro954Ser
ENST00000393347.7:c.2860C>T	ENSP00000377016.3:p.Pro954Ser
ENST00000502649.5:c.2860C>T	ENSP00000426057.1:p.Pro954Ser
ENST00000507059.5:n.2253C>T
ENST00000512795.1:c.-27C>T	ENSP00000421535.1:n.-27C>T
ENST00000514810.1:n.227C>T
ENST00000619105.4:c.*1803C>T	ENSP00000481134.1:n.*1803C>T
NM_002020.4:c.2860C>T	NP_002011.2:p.Pro954Ser
NM_182925.4:c.2860C>T	NP_891555.2:p.Pro954Ser
XM_011534477.1:c.3109C>T	XP_011532779.1:p.Pro1037Ser
XM_011534478.1:c.3091C>T	XP_011532780.1:p.Pro1031Ser
XM_011534479.1:c.3109C>T	XP_011532781.1:p.Pro1037Ser
XM_011534480.1:c.3109C>T	XP_011532782.1:p.Pro1037Ser
XM_011534481.1:c.3109C>T	XP_011532783.1:p.Pro1037Ser
XM_011534482.1:c.2878C>T	XP_011532784.1:p.Pro960Ser
XM_011534483.1:c.2800C>T	XP_011532785.1:p.Pro934Ser
XM_011534484.1:c.2401C>T	XP_011532786.1:p.Pro801Ser
XR_941095.1:n.3121C>T
NM_001354989.1:c.2860C>T	NP_001341918.1:p.Pro954Ser
XM_011534478.3:c.3091C>T	XP_011532780.1:p.Pro1031Ser
XM_011534484.2:c.2401C>T	XP_011532786.1:p.Pro801Ser
XM_017009263.1:c.3091C>T	XP_016864752.1:p.Pro1031Ser
XM_017009264.2:c.3091C>T	XP_016864753.1:p.Pro1031Ser
XM_017009265.1:c.3091C>T	XP_016864754.1:p.Pro1031Ser
XM_017009266.1:c.3091C>T	XP_016864755.1:p.Pro1031Ser
XM_017009267.2:c.3091C>T	XP_016864756.1:p.Pro1031Ser
XM_017009268.1:c.2782C>T	XP_016864757.1:p.Pro928Ser
XR_001742050.2:n.3325C>T
NM_182925.5:c.2860C>T MANE Select	NP_891555.2:p.Pro954Ser
NM_001354989.2:c.2860C>T	NP_001341918.1:p.Pro954Ser
NM_002020.5:c.2860C>T	NP_002011.2:p.Pro954Ser