Canonical Allele Identifier: CA448099064

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030309C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603309C>T , CM000667.2:g.180603309C>T	GRCh38
NC_000005.9:g.180030309C>T , CM000667.1:g.180030309C>T	GRCh37
NC_000005.8:g.179962915C>T	NCBI36
NG_011536.1:g.51316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3975G>A MANE Select	ENSP00000261937.6:p.Gly1325=
ENST00000261937.10:c.3975G>A	ENSP00000261937.6:p.Gly1325=
ENST00000502603.5:n.675G>A
NM_182925.4:c.3975G>A	NP_891555.2:p.Gly1325=
XM_011534477.1:c.4224G>A	XP_011532779.1:p.Gly1408=
XM_011534478.1:c.4206G>A	XP_011532780.1:p.Gly1402=
XM_011534479.1:c.*121G>A	XP_011532781.1:n.*121G>A
XM_011534482.1:c.3993G>A	XP_011532784.1:p.Gly1331=
XM_011534483.1:c.3915G>A	XP_011532785.1:p.Gly1305=
XM_011534484.1:c.3516G>A	XP_011532786.1:p.Gly1172=
XR_941095.1:n.4261G>A
XM_011534478.3:c.4206G>A	XP_011532780.1:p.Gly1402=
XM_011534484.2:c.3516G>A	XP_011532786.1:p.Gly1172=
XM_017009263.1:c.*121G>A	XP_016864752.1:n.*121G>A
XM_017009268.1:c.3897G>A	XP_016864757.1:p.Gly1299=
XR_001742050.2:n.4465G>A
NM_182925.5:c.3975G>A MANE Select	NP_891555.2:p.Gly1325=