Canonical Allele Identifier: CA1604723033

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619624C= , CM000667.2:g.180619624C=	GRCh38
NC_000005.9:g.180046624C= , CM000667.1:g.180046624C=	GRCh37
NC_000005.8:g.179979230C=	NCBI36
NG_011536.1:g.35001G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2647+41G= MANE Select	ENSP00000261937.6:n.2647+41G=
ENST00000261937.10:c.2647+41G=	ENSP00000261937.6:n.2647+41G=
ENST00000393347.7:c.2647+41G=	ENSP00000377016.3:n.2647+41G=
ENST00000502649.5:c.2647+41G=	ENSP00000426057.1:n.2647+41G=
ENST00000507059.5:n.1783G=
ENST00000619105.4:c.*1590+41G=	ENSP00000481134.1:n.*1590+41G=
NM_002020.4:c.2647+41G=	NP_002011.2:n.2647+41G=
NM_182925.4:c.2647+41G=	NP_891555.2:n.2647+41G=
XM_011534477.1:c.2896+41G=	XP_011532779.1:n.2896+41G=
XM_011534478.1:c.2878+41G=	XP_011532780.1:n.2878+41G=
XM_011534479.1:c.2896+41G=	XP_011532781.1:n.2896+41G=
XM_011534480.1:c.2896+41G=	XP_011532782.1:n.2896+41G=
XM_011534481.1:c.2896+41G=	XP_011532783.1:n.2896+41G=
XM_011534482.1:c.2665+41G=	XP_011532784.1:n.2665+41G=
XM_011534483.1:c.2587+41G=	XP_011532785.1:n.2587+41G=
XM_011534484.1:c.2188+41G=	XP_011532786.1:n.2188+41G=
XR_941095.1:n.2908+41G=
NM_001354989.1:c.2647+41G=	NP_001341918.1:n.2647+41G=
XM_011534478.3:c.2878+41G=	XP_011532780.1:n.2878+41G=
XM_011534484.2:c.2188+41G=	XP_011532786.1:n.2188+41G=
XM_017009263.1:c.2878+41G=	XP_016864752.1:n.2878+41G=
XM_017009264.2:c.2878+41G=	XP_016864753.1:n.2878+41G=
XM_017009265.1:c.2878+41G=	XP_016864754.1:n.2878+41G=
XM_017009266.1:c.2878+41G=	XP_016864755.1:n.2878+41G=
XM_017009267.2:c.2878+41G=	XP_016864756.1:n.2878+41G=
XM_017009268.1:c.2569+41G=	XP_016864757.1:n.2569+41G=
XR_001742050.2:n.3112+41G=
NM_182925.5:c.2647+41G= MANE Select	NP_891555.2:n.2647+41G=
NM_001354989.2:c.2647+41G=	NP_001341918.1:n.2647+41G=
NM_002020.5:c.2647+41G=	NP_002011.2:n.2647+41G=