Canonical Allele Identifier: CA133199475

Gene: FLT4

Linked Data

• ClinVar Variation Id: 2292955
• ClinVar RCV Id: RCV002873003
• dbSNP Id: rs746207295
• gnomAD v2: 5-180036934-T-C
• gnomAD v3: 5-180609934-T-C
• gnomAD v4: 5-180609934-T-C
• MyVariant Identifiers: chr5:g.180036934T>C (hg19) ; chr5:g.180609934T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609934T>C , CM000667.2:g.180609934T>C	GRCh38
NC_000005.9:g.180036934T>C , CM000667.1:g.180036934T>C	GRCh37
NC_000005.8:g.179969540T>C	NCBI36
NG_011536.1:g.44691A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3778A>G MANE Select	ENSP00000261937.6:p.Met1260Val
ENST00000261937.10:c.3778A>G	ENSP00000261937.6:p.Met1260Val
ENST00000393347.7:c.3778A>G	ENSP00000377016.3:p.Met1260Val
ENST00000502603.5:n.478A>G
ENST00000502649.5:c.3778A>G	ENSP00000426057.1:p.Met1260Val
ENST00000507059.5:n.4128A>G
ENST00000619105.4:c.*2721A>G	ENSP00000481134.1:n.*2721A>G
NM_002020.4:c.3778A>G	NP_002011.2:p.Met1260Val
NM_182925.4:c.3778A>G	NP_891555.2:p.Met1260Val
XM_011534477.1:c.4027A>G	XP_011532779.1:p.Met1343Val
XM_011534478.1:c.4009A>G	XP_011532780.1:p.Met1337Val
XM_011534479.1:c.4027A>G	XP_011532781.1:p.Met1343Val
XM_011534480.1:c.4027A>G	XP_011532782.1:p.Met1343Val
XM_011534481.1:c.4027A>G	XP_011532783.1:p.Met1343Val
XM_011534482.1:c.3796A>G	XP_011532784.1:p.Met1266Val
XM_011534483.1:c.3718A>G	XP_011532785.1:p.Met1240Val
XM_011534484.1:c.3319A>G	XP_011532786.1:p.Met1107Val
XR_941095.1:n.4064A>G
NM_001354989.1:c.3778A>G	NP_001341918.1:p.Met1260Val
XM_011534478.3:c.4009A>G	XP_011532780.1:p.Met1337Val
XM_011534484.2:c.3319A>G	XP_011532786.1:p.Met1107Val
XM_017009263.1:c.4009A>G	XP_016864752.1:p.Met1337Val
XM_017009264.2:c.4009A>G	XP_016864753.1:p.Met1337Val
XM_017009265.1:c.4009A>G	XP_016864754.1:p.Met1337Val
XM_017009266.1:c.4009A>G	XP_016864755.1:p.Met1337Val
XM_017009267.2:c.4009A>G	XP_016864756.1:p.Met1337Val
XM_017009268.1:c.3700A>G	XP_016864757.1:p.Met1234Val
XR_001742050.2:n.4268A>G
NM_182925.5:c.3778A>G MANE Select	NP_891555.2:p.Met1260Val
NM_001354989.2:c.3778A>G	NP_001341918.1:p.Met1260Val
NM_002020.5:c.3778A>G	NP_002011.2:p.Met1260Val