Canonical Allele Identifier: CA362496343

Gene: FLT4

Linked Data

• dbSNP Id: rs1382151235
• gnomAD v2: 5-180030382-C-T
• gnomAD v3: 5-180603382-C-T
• gnomAD v4: 5-180603382-C-T
• MyVariant Identifiers: chr5:g.180030382C>T (hg19) ; chr5:g.180603382C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603382C>T , CM000667.2:g.180603382C>T	GRCh38
NC_000005.9:g.180030382C>T , CM000667.1:g.180030382C>T	GRCh37
NC_000005.8:g.179962988C>T	NCBI36
NG_011536.1:g.51243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3902G>A MANE Select	ENSP00000261937.6:p.Gly1301Glu
ENST00000261937.10:c.3902G>A	ENSP00000261937.6:p.Gly1301Glu
ENST00000502603.5:n.602G>A
NM_182925.4:c.3902G>A	NP_891555.2:p.Gly1301Glu
XM_011534477.1:c.4151G>A	XP_011532779.1:p.Gly1384Glu
XM_011534478.1:c.4133G>A	XP_011532780.1:p.Gly1378Glu
XM_011534479.1:c.*48G>A	XP_011532781.1:n.*48G>A
XM_011534482.1:c.3920G>A	XP_011532784.1:p.Gly1307Glu
XM_011534483.1:c.3842G>A	XP_011532785.1:p.Gly1281Glu
XM_011534484.1:c.3443G>A	XP_011532786.1:p.Gly1148Glu
XR_941095.1:n.4188G>A
XM_011534478.3:c.4133G>A	XP_011532780.1:p.Gly1378Glu
XM_011534484.2:c.3443G>A	XP_011532786.1:p.Gly1148Glu
XM_017009263.1:c.*48G>A	XP_016864752.1:n.*48G>A
XM_017009268.1:c.3824G>A	XP_016864757.1:p.Gly1275Glu
XR_001742050.2:n.4392G>A
NM_182925.5:c.3902G>A MANE Select	NP_891555.2:p.Gly1301Glu