Canonical Allele Identifier: CA3605580

Gene: FLT4

Linked Data

• dbSNP Id: rs762533367
• ExAC: 5:180030222 G / A
• gnomAD v2: 5-180030222-G-A
• gnomAD v3: 5-180603222-G-A
• gnomAD v4: 5-180603222-G-A
• MyVariant Identifiers: chr5:g.180030222G>A (hg19) ; chr5:g.180603222G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603222G>A , CM000667.2:g.180603222G>A	GRCh38
NC_000005.9:g.180030222G>A , CM000667.1:g.180030222G>A	GRCh37
NC_000005.8:g.179962828G>A	NCBI36
NG_011536.1:g.51403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4062C>T MANE Select	ENSP00000261937.6:p.Arg1354=
ENST00000261937.10:c.4062C>T	ENSP00000261937.6:p.Arg1354=
ENST00000502603.5:n.762C>T
NM_182925.4:c.4062C>T	NP_891555.2:p.Arg1354=
XM_011534477.1:c.4311C>T	XP_011532779.1:p.Arg1437=
XM_011534478.1:c.4293C>T	XP_011532780.1:p.Arg1431=
XM_011534482.1:c.4080C>T	XP_011532784.1:p.Arg1360=
XM_011534483.1:c.4002C>T	XP_011532785.1:p.Arg1334=
XM_011534484.1:c.3603C>T	XP_011532786.1:p.Arg1201=
XR_941095.1:n.4348C>T
XM_011534478.3:c.4293C>T	XP_011532780.1:p.Arg1431=
XM_011534484.2:c.3603C>T	XP_011532786.1:p.Arg1201=
XM_017009263.1:c.*208C>T	XP_016864752.1:n.*208C>T
XM_017009268.1:c.3984C>T	XP_016864757.1:p.Arg1328=
XR_001742050.2:n.4552C>T
NM_182925.5:c.4062C>T MANE Select	NP_891555.2:p.Arg1354=