Canonical Allele Identifier: CA362496097

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030338G>A (hg19) ; chr5:g.180603338G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603338G>A , CM000667.2:g.180603338G>A	GRCh38
NC_000005.9:g.180030338G>A , CM000667.1:g.180030338G>A	GRCh37
NC_000005.8:g.179962944G>A	NCBI36
NG_011536.1:g.51287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3946C>T MANE Select	ENSP00000261937.6:p.Gln1316Ter
ENST00000261937.10:c.3946C>T	ENSP00000261937.6:p.Gln1316Ter
ENST00000502603.5:n.646C>T
NM_182925.4:c.3946C>T	NP_891555.2:p.Gln1316Ter
XM_011534477.1:c.4195C>T	XP_011532779.1:p.Gln1399Ter
XM_011534478.1:c.4177C>T	XP_011532780.1:p.Gln1393Ter
XM_011534479.1:c.*92C>T	XP_011532781.1:n.*92C>T
XM_011534482.1:c.3964C>T	XP_011532784.1:p.Gln1322Ter
XM_011534483.1:c.3886C>T	XP_011532785.1:p.Gln1296Ter
XM_011534484.1:c.3487C>T	XP_011532786.1:p.Gln1163Ter
XR_941095.1:n.4232C>T
XM_011534478.3:c.4177C>T	XP_011532780.1:p.Gln1393Ter
XM_011534484.2:c.3487C>T	XP_011532786.1:p.Gln1163Ter
XM_017009263.1:c.*92C>T	XP_016864752.1:n.*92C>T
XM_017009268.1:c.3868C>T	XP_016864757.1:p.Gln1290Ter
XR_001742050.2:n.4436C>T
NM_182925.5:c.3946C>T MANE Select	NP_891555.2:p.Gln1316Ter