Canonical Allele Identifier: CA448098925

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030207T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603207T>A , CM000667.2:g.180603207T>A	GRCh38
NC_000005.9:g.180030207T>A , CM000667.1:g.180030207T>A	GRCh37
NC_000005.8:g.179962813T>A	NCBI36
NG_011536.1:g.51418A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4077A>T MANE Select	ENSP00000261937.6:p.Thr1359=
ENST00000261937.10:c.4077A>T	ENSP00000261937.6:p.Thr1359=
ENST00000502603.5:n.777A>T
NM_182925.4:c.4077A>T	NP_891555.2:p.Thr1359=
XM_011534477.1:c.4326A>T	XP_011532779.1:p.Thr1442=
XM_011534478.1:c.4308A>T	XP_011532780.1:p.Thr1436=
XM_011534482.1:c.4095A>T	XP_011532784.1:p.Thr1365=
XM_011534483.1:c.4017A>T	XP_011532785.1:p.Thr1339=
XM_011534484.1:c.3618A>T	XP_011532786.1:p.Thr1206=
XR_941095.1:n.4363A>T
XM_011534478.3:c.4308A>T	XP_011532780.1:p.Thr1436=
XM_011534484.2:c.3618A>T	XP_011532786.1:p.Thr1206=
XM_017009263.1:c.*223A>T	XP_016864752.1:n.*223A>T
XM_017009268.1:c.3999A>T	XP_016864757.1:p.Thr1333=
XR_001742050.2:n.4567A>T
NM_182925.5:c.4077A>T MANE Select	NP_891555.2:p.Thr1359=