Canonical Allele Identifier: CA3605578

Gene: FLT4

Linked Data

• dbSNP Id: rs769432789
• ExAC: 5:180030214 A / G
• gnomAD v2: 5-180030214-A-G
• gnomAD v4: 5-180603214-A-G
• MyVariant Identifiers: chr5:g.180030214A>G (hg19) ; chr5:g.180603214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603214A>G , CM000667.2:g.180603214A>G	GRCh38
NC_000005.9:g.180030214A>G , CM000667.1:g.180030214A>G	GRCh37
NC_000005.8:g.179962820A>G	NCBI36
NG_011536.1:g.51411T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4070T>C MANE Select	ENSP00000261937.6:p.Phe1357Ser
ENST00000261937.10:c.4070T>C	ENSP00000261937.6:p.Phe1357Ser
ENST00000502603.5:n.770T>C
NM_182925.4:c.4070T>C	NP_891555.2:p.Phe1357Ser
XM_011534477.1:c.4319T>C	XP_011532779.1:p.Phe1440Ser
XM_011534478.1:c.4301T>C	XP_011532780.1:p.Phe1434Ser
XM_011534482.1:c.4088T>C	XP_011532784.1:p.Phe1363Ser
XM_011534483.1:c.4010T>C	XP_011532785.1:p.Phe1337Ser
XM_011534484.1:c.3611T>C	XP_011532786.1:p.Phe1204Ser
XR_941095.1:n.4356T>C
XM_011534478.3:c.4301T>C	XP_011532780.1:p.Phe1434Ser
XM_011534484.2:c.3611T>C	XP_011532786.1:p.Phe1204Ser
XM_017009263.1:c.*216T>C	XP_016864752.1:n.*216T>C
XM_017009268.1:c.3992T>C	XP_016864757.1:p.Phe1331Ser
XR_001742050.2:n.4560T>C
NM_182925.5:c.4070T>C MANE Select	NP_891555.2:p.Phe1357Ser