Canonical Allele Identifier: CA448099089

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030333C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603333C>A , CM000667.2:g.180603333C>A	GRCh38
NC_000005.9:g.180030333C>A , CM000667.1:g.180030333C>A	GRCh37
NC_000005.8:g.179962939C>A	NCBI36
NG_011536.1:g.51292G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3951G>T MANE Select	ENSP00000261937.6:p.Gly1317=
ENST00000261937.10:c.3951G>T	ENSP00000261937.6:p.Gly1317=
ENST00000502603.5:n.651G>T
NM_182925.4:c.3951G>T	NP_891555.2:p.Gly1317=
XM_011534477.1:c.4200G>T	XP_011532779.1:p.Gly1400=
XM_011534478.1:c.4182G>T	XP_011532780.1:p.Gly1394=
XM_011534479.1:c.*97G>T	XP_011532781.1:n.*97G>T
XM_011534482.1:c.3969G>T	XP_011532784.1:p.Gly1323=
XM_011534483.1:c.3891G>T	XP_011532785.1:p.Gly1297=
XM_011534484.1:c.3492G>T	XP_011532786.1:p.Gly1164=
XR_941095.1:n.4237G>T
XM_011534478.3:c.4182G>T	XP_011532780.1:p.Gly1394=
XM_011534484.2:c.3492G>T	XP_011532786.1:p.Gly1164=
XM_017009263.1:c.*97G>T	XP_016864752.1:n.*97G>T
XM_017009268.1:c.3873G>T	XP_016864757.1:p.Gly1291=
XR_001742050.2:n.4441G>T
NM_182925.5:c.3951G>T MANE Select	NP_891555.2:p.Gly1317=