Canonical Allele Identifier: CA3605623

Gene: FLT4

Linked Data

• dbSNP Id: rs142322370
• ExAC: 5:180030329 G / A
• gnomAD v2: 5-180030329-G-A
• gnomAD v3: 5-180603329-G-A
• gnomAD v4: 5-180603329-G-A
• COSMIC: COSM244558
• MyVariant Identifiers: chr5:g.180030329G>A (hg19) ; chr5:g.180603329G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603329G>A , CM000667.2:g.180603329G>A	GRCh38
NC_000005.9:g.180030329G>A , CM000667.1:g.180030329G>A	GRCh37
NC_000005.8:g.179962935G>A	NCBI36
NG_011536.1:g.51296C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3955C>T MANE Select	ENSP00000261937.6:p.Arg1319Trp
ENST00000261937.10:c.3955C>T	ENSP00000261937.6:p.Arg1319Trp
ENST00000502603.5:n.655C>T
NM_182925.4:c.3955C>T	NP_891555.2:p.Arg1319Trp
XM_011534477.1:c.4204C>T	XP_011532779.1:p.Arg1402Trp
XM_011534478.1:c.4186C>T	XP_011532780.1:p.Arg1396Trp
XM_011534479.1:c.*101C>T	XP_011532781.1:n.*101C>T
XM_011534482.1:c.3973C>T	XP_011532784.1:p.Arg1325Trp
XM_011534483.1:c.3895C>T	XP_011532785.1:p.Arg1299Trp
XM_011534484.1:c.3496C>T	XP_011532786.1:p.Arg1166Trp
XR_941095.1:n.4241C>T
XM_011534478.3:c.4186C>T	XP_011532780.1:p.Arg1396Trp
XM_011534484.2:c.3496C>T	XP_011532786.1:p.Arg1166Trp
XM_017009263.1:c.*101C>T	XP_016864752.1:n.*101C>T
XM_017009268.1:c.3877C>T	XP_016864757.1:p.Arg1293Trp
XR_001742050.2:n.4445C>T
NM_182925.5:c.3955C>T MANE Select	NP_891555.2:p.Arg1319Trp