Canonical Allele Identifier: CA3605591

Gene: FLT4

Linked Data

• dbSNP Id: rs746834315
• ExAC: 5:180030248 C / G
• gnomAD v2: 5-180030248-C-G
• gnomAD v4: 5-180603248-C-G
• MyVariant Identifiers: chr5:g.180030248C>G (hg19) ; chr5:g.180603248C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603248C>G , CM000667.2:g.180603248C>G	GRCh38
NC_000005.9:g.180030248C>G , CM000667.1:g.180030248C>G	GRCh37
NC_000005.8:g.179962854C>G	NCBI36
NG_011536.1:g.51377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4036G>C MANE Select	ENSP00000261937.6:p.Glu1346Gln
ENST00000261937.10:c.4036G>C	ENSP00000261937.6:p.Glu1346Gln
ENST00000502603.5:n.736G>C
NM_182925.4:c.4036G>C	NP_891555.2:p.Glu1346Gln
XM_011534477.1:c.4285G>C	XP_011532779.1:p.Glu1429Gln
XM_011534478.1:c.4267G>C	XP_011532780.1:p.Glu1423Gln
XM_011534482.1:c.4054G>C	XP_011532784.1:p.Glu1352Gln
XM_011534483.1:c.3976G>C	XP_011532785.1:p.Glu1326Gln
XM_011534484.1:c.3577G>C	XP_011532786.1:p.Glu1193Gln
XR_941095.1:n.4322G>C
XM_011534478.3:c.4267G>C	XP_011532780.1:p.Glu1423Gln
XM_011534484.2:c.3577G>C	XP_011532786.1:p.Glu1193Gln
XM_017009263.1:c.*182G>C	XP_016864752.1:n.*182G>C
XM_017009268.1:c.3958G>C	XP_016864757.1:p.Glu1320Gln
XR_001742050.2:n.4526G>C
NM_182925.5:c.4036G>C MANE Select	NP_891555.2:p.Glu1346Gln