Canonical Allele Identifier: CA362495375

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030212A>T (hg19) ; chr5:g.180603212A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603212A>T , CM000667.2:g.180603212A>T	GRCh38
NC_000005.9:g.180030212A>T , CM000667.1:g.180030212A>T	GRCh37
NC_000005.8:g.179962818A>T	NCBI36
NG_011536.1:g.51413T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4072T>A MANE Select	ENSP00000261937.6:p.Phe1358Ile
ENST00000261937.10:c.4072T>A	ENSP00000261937.6:p.Phe1358Ile
ENST00000502603.5:n.772T>A
NM_182925.4:c.4072T>A	NP_891555.2:p.Phe1358Ile
XM_011534477.1:c.4321T>A	XP_011532779.1:p.Phe1441Ile
XM_011534478.1:c.4303T>A	XP_011532780.1:p.Phe1435Ile
XM_011534482.1:c.4090T>A	XP_011532784.1:p.Phe1364Ile
XM_011534483.1:c.4012T>A	XP_011532785.1:p.Phe1338Ile
XM_011534484.1:c.3613T>A	XP_011532786.1:p.Phe1205Ile
XR_941095.1:n.4358T>A
XM_011534478.3:c.4303T>A	XP_011532780.1:p.Phe1435Ile
XM_011534484.2:c.3613T>A	XP_011532786.1:p.Phe1205Ile
XM_017009263.1:c.*218T>A	XP_016864752.1:n.*218T>A
XM_017009268.1:c.3994T>A	XP_016864757.1:p.Phe1332Ile
XR_001742050.2:n.4562T>A
NM_182925.5:c.4072T>A MANE Select	NP_891555.2:p.Phe1358Ile