Canonical Allele Identifier: CA362495946

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030307G>T (hg19) ; chr5:g.180603307G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603307G>T , CM000667.2:g.180603307G>T	GRCh38
NC_000005.9:g.180030307G>T , CM000667.1:g.180030307G>T	GRCh37
NC_000005.8:g.179962913G>T	NCBI36
NG_011536.1:g.51318C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3977C>A MANE Select	ENSP00000261937.6:p.Ala1326Asp
ENST00000261937.10:c.3977C>A	ENSP00000261937.6:p.Ala1326Asp
ENST00000502603.5:n.677C>A
NM_182925.4:c.3977C>A	NP_891555.2:p.Ala1326Asp
XM_011534477.1:c.4226C>A	XP_011532779.1:p.Ala1409Asp
XM_011534478.1:c.4208C>A	XP_011532780.1:p.Ala1403Asp
XM_011534479.1:c.*123C>A	XP_011532781.1:n.*123C>A
XM_011534482.1:c.3995C>A	XP_011532784.1:p.Ala1332Asp
XM_011534483.1:c.3917C>A	XP_011532785.1:p.Ala1306Asp
XM_011534484.1:c.3518C>A	XP_011532786.1:p.Ala1173Asp
XR_941095.1:n.4263C>A
XM_011534478.3:c.4208C>A	XP_011532780.1:p.Ala1403Asp
XM_011534484.2:c.3518C>A	XP_011532786.1:p.Ala1173Asp
XM_017009263.1:c.*123C>A	XP_016864752.1:n.*123C>A
XM_017009268.1:c.3899C>A	XP_016864757.1:p.Ala1300Asp
XR_001742050.2:n.4467C>A
NM_182925.5:c.3977C>A MANE Select	NP_891555.2:p.Ala1326Asp