Canonical Allele Identifier: CA3605604

Gene: FLT4

Linked Data

• dbSNP Id: rs765704568
• ExAC: 5:180030299 C / T
• gnomAD v2: 5-180030299-C-T
• gnomAD v3: 5-180603299-C-T
• gnomAD v4: 5-180603299-C-T
• MyVariant Identifiers: chr5:g.180030299C>T (hg19) ; chr5:g.180603299C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603299C>T , CM000667.2:g.180603299C>T	GRCh38
NC_000005.9:g.180030299C>T , CM000667.1:g.180030299C>T	GRCh37
NC_000005.8:g.179962905C>T	NCBI36
NG_011536.1:g.51326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3985G>A MANE Select	ENSP00000261937.6:p.Gly1329Ser
ENST00000261937.10:c.3985G>A	ENSP00000261937.6:p.Gly1329Ser
ENST00000502603.5:n.685G>A
NM_182925.4:c.3985G>A	NP_891555.2:p.Gly1329Ser
XM_011534477.1:c.4234G>A	XP_011532779.1:p.Gly1412Ser
XM_011534478.1:c.4216G>A	XP_011532780.1:p.Gly1406Ser
XM_011534482.1:c.4003G>A	XP_011532784.1:p.Gly1335Ser
XM_011534483.1:c.3925G>A	XP_011532785.1:p.Gly1309Ser
XM_011534484.1:c.3526G>A	XP_011532786.1:p.Gly1176Ser
XR_941095.1:n.4271G>A
XM_011534478.3:c.4216G>A	XP_011532780.1:p.Gly1406Ser
XM_011534484.2:c.3526G>A	XP_011532786.1:p.Gly1176Ser
XM_017009263.1:c.*131G>A	XP_016864752.1:n.*131G>A
XM_017009268.1:c.3907G>A	XP_016864757.1:p.Gly1303Ser
XR_001742050.2:n.4475G>A
NM_182925.5:c.3985G>A MANE Select	NP_891555.2:p.Gly1329Ser