Canonical Allele Identifier: CA362495602

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030258C>A (hg19) ; chr5:g.180603258C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603258C>A , CM000667.2:g.180603258C>A	GRCh38
NC_000005.9:g.180030258C>A , CM000667.1:g.180030258C>A	GRCh37
NC_000005.8:g.179962864C>A	NCBI36
NG_011536.1:g.51367G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4026G>T MANE Select	ENSP00000261937.6:p.Glu1342Asp
ENST00000261937.10:c.4026G>T	ENSP00000261937.6:p.Glu1342Asp
ENST00000502603.5:n.726G>T
NM_182925.4:c.4026G>T	NP_891555.2:p.Glu1342Asp
XM_011534477.1:c.4275G>T	XP_011532779.1:p.Glu1425Asp
XM_011534478.1:c.4257G>T	XP_011532780.1:p.Glu1419Asp
XM_011534482.1:c.4044G>T	XP_011532784.1:p.Glu1348Asp
XM_011534483.1:c.3966G>T	XP_011532785.1:p.Glu1322Asp
XM_011534484.1:c.3567G>T	XP_011532786.1:p.Glu1189Asp
XR_941095.1:n.4312G>T
XM_011534478.3:c.4257G>T	XP_011532780.1:p.Glu1419Asp
XM_011534484.2:c.3567G>T	XP_011532786.1:p.Glu1189Asp
XM_017009263.1:c.*172G>T	XP_016864752.1:n.*172G>T
XM_017009268.1:c.3948G>T	XP_016864757.1:p.Glu1316Asp
XR_001742050.2:n.4516G>T
NM_182925.5:c.4026G>T MANE Select	NP_891555.2:p.Glu1342Asp