Canonical Allele Identifier: CA3607228

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180631720G>A , CM000667.2:g.180631720G>A	GRCh38
NC_000005.9:g.180058720G>A , CM000667.1:g.180058720G>A	GRCh37
NC_000005.8:g.179991326G>A	NCBI36
NG_011536.1:g.22905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.117C>T MANE Select	ENSP00000261937.6:p.His39=
ENST00000261937.10:c.117C>T	ENSP00000261937.6:p.His39=
ENST00000393347.7:c.117C>T	ENSP00000377016.3:p.His39=
ENST00000424276.6:n.117C>T
ENST00000502293.5:n.117C>T
ENST00000502649.5:c.117C>T	ENSP00000426057.1:p.His39=
ENST00000513527.1:n.117C>T
ENST00000619105.4:c.117C>T	ENSP00000481134.1:p.His39=
NM_002020.4:c.117C>T	NP_002011.2:p.His39=
NM_182925.4:c.117C>T	NP_891555.2:p.His39=
XM_011534477.1:c.348C>T	XP_011532779.1:p.His116=
XM_011534478.1:c.348C>T	XP_011532780.1:p.His116=
XM_011534479.1:c.348C>T	XP_011532781.1:p.His116=
XM_011534480.1:c.348C>T	XP_011532782.1:p.His116=
XM_011534481.1:c.348C>T	XP_011532783.1:p.His116=
XM_011534482.1:c.117C>T	XP_011532784.1:p.His39=
XM_011534483.1:c.39C>T	XP_011532785.1:p.His13=
XR_941095.1:n.360C>T
NM_001354989.1:c.117C>T	NP_001341918.1:p.His39=
XM_011534478.3:c.348C>T	XP_011532780.1:p.His116=
XM_017009263.1:c.348C>T	XP_016864752.1:p.His116=
XM_017009264.2:c.348C>T	XP_016864753.1:p.His116=
XM_017009265.1:c.348C>T	XP_016864754.1:p.His116=
XM_017009266.1:c.348C>T	XP_016864755.1:p.His116=
XM_017009267.2:c.348C>T	XP_016864756.1:p.His116=
XM_017009268.1:c.39C>T	XP_016864757.1:p.His13=
XR_001742050.2:n.582C>T
NM_182925.5:c.117C>T MANE Select	NP_891555.2:p.His39=
NM_001354989.2:c.117C>T	NP_001341918.1:p.His39=
NM_002020.5:c.117C>T	NP_002011.2:p.His39=