Canonical Allele Identifier: CA362501374

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619100A>T , CM000667.2:g.180619100A>T	GRCh38
NC_000005.9:g.180046100A>T , CM000667.1:g.180046100A>T	GRCh37
NC_000005.8:g.179978706A>T	NCBI36
NG_011536.1:g.35525T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_182925.5:c.2771T>A MANE Select	NP_891555.2:p.Met924Lys
ENST00000261937.11:c.2771T>A MANE Select	ENSP00000261937.6:p.Met924Lys
NM_001354989.1:c.2771T>A	NP_001341918.1:p.Met924Lys
NM_001354989.2:c.2771T>A	NP_001341918.1:p.Met924Lys
NM_002020.4:c.2771T>A	NP_002011.2:p.Met924Lys
NM_002020.5:c.2771T>A	NP_002011.2:p.Met924Lys
NM_182925.4:c.2771T>A	NP_891555.2:p.Met924Lys
ENST00000261937.10:c.2771T>A	ENSP00000261937.6:p.Met924Lys
ENST00000393347.7:c.2771T>A	ENSP00000377016.3:p.Met924Lys
ENST00000502649.5:c.2771T>A	ENSP00000426057.1:p.Met924Lys
ENST00000507059.5:n.2164T>A
ENST00000512795.1:c.-37+153T>A	ENSP00000421535.1:n.-37+153T>A
ENST00000514810.1:n.38T>A
ENST00000619105.4:c.*1714T>A	ENSP00000481134.1:n.*1714T>A
XM_011534477.1:c.3020T>A	XP_011532779.1:p.Met1007Lys
XM_011534478.1:c.3002T>A	XP_011532780.1:p.Met1001Lys
XM_011534478.3:c.3002T>A	XP_011532780.1:p.Met1001Lys
XM_011534479.1:c.3020T>A	XP_011532781.1:p.Met1007Lys
XM_011534480.1:c.3020T>A	XP_011532782.1:p.Met1007Lys
XM_011534481.1:c.3020T>A	XP_011532783.1:p.Met1007Lys
XM_011534482.1:c.2789T>A	XP_011532784.1:p.Met930Lys
XM_011534483.1:c.2711T>A	XP_011532785.1:p.Met904Lys
XM_011534484.1:c.2312T>A	XP_011532786.1:p.Met771Lys
XM_011534484.2:c.2312T>A	XP_011532786.1:p.Met771Lys
XM_017009263.1:c.3002T>A	XP_016864752.1:p.Met1001Lys
XM_017009264.2:c.3002T>A	XP_016864753.1:p.Met1001Lys
XM_017009265.1:c.3002T>A	XP_016864754.1:p.Met1001Lys
XM_017009266.1:c.3002T>A	XP_016864755.1:p.Met1001Lys
XM_017009267.2:c.3002T>A	XP_016864756.1:p.Met1001Lys
XM_017009268.1:c.2693T>A	XP_016864757.1:p.Met898Lys
XR_001742050.2:n.3236T>A
XR_941095.1:n.3032T>A