Canonical Allele Identifier: CA362500138

Gene: FLT4

Linked Data

• gnomAD v4: 5-180614080-T-C
• MyVariant Identifiers: chr5:g.180041080T>C (hg19) ; chr5:g.180614080T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614080T>C , CM000667.2:g.180614080T>C	GRCh38
NC_000005.9:g.180041080T>C , CM000667.1:g.180041080T>C	GRCh37
NC_000005.8:g.179973686T>C	NCBI36
NG_011536.1:g.40545A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3319A>G MANE Select	ENSP00000261937.6:p.Ile1107Val
ENST00000261937.10:c.3319A>G	ENSP00000261937.6:p.Ile1107Val
ENST00000393347.7:c.3319A>G	ENSP00000377016.3:p.Ile1107Val
ENST00000502649.5:c.3319A>G	ENSP00000426057.1:p.Ile1107Val
ENST00000507059.5:n.2712A>G
ENST00000514810.1:n.686A>G
ENST00000619105.4:c.*2262A>G	ENSP00000481134.1:n.*2262A>G
NM_002020.4:c.3319A>G	NP_002011.2:p.Ile1107Val
NM_182925.4:c.3319A>G	NP_891555.2:p.Ile1107Val
XM_011534477.1:c.3568A>G	XP_011532779.1:p.Ile1190Val
XM_011534478.1:c.3550A>G	XP_011532780.1:p.Ile1184Val
XM_011534479.1:c.3568A>G	XP_011532781.1:p.Ile1190Val
XM_011534480.1:c.3568A>G	XP_011532782.1:p.Ile1190Val
XM_011534481.1:c.3568A>G	XP_011532783.1:p.Ile1190Val
XM_011534482.1:c.3337A>G	XP_011532784.1:p.Ile1113Val
XM_011534483.1:c.3259A>G	XP_011532785.1:p.Ile1087Val
XM_011534484.1:c.2860A>G	XP_011532786.1:p.Ile954Val
XR_941095.1:n.3580A>G
NM_001354989.1:c.3319A>G	NP_001341918.1:p.Ile1107Val
XM_011534478.3:c.3550A>G	XP_011532780.1:p.Ile1184Val
XM_011534484.2:c.2860A>G	XP_011532786.1:p.Ile954Val
XM_017009263.1:c.3550A>G	XP_016864752.1:p.Ile1184Val
XM_017009264.2:c.3550A>G	XP_016864753.1:p.Ile1184Val
XM_017009265.1:c.3550A>G	XP_016864754.1:p.Ile1184Val
XM_017009266.1:c.3550A>G	XP_016864755.1:p.Ile1184Val
XM_017009267.2:c.3550A>G	XP_016864756.1:p.Ile1184Val
XM_017009268.1:c.3241A>G	XP_016864757.1:p.Ile1081Val
XR_001742050.2:n.3784A>G
NM_182925.5:c.3319A>G MANE Select	NP_891555.2:p.Ile1107Val
NM_001354989.2:c.3319A>G	NP_001341918.1:p.Ile1107Val
NM_002020.5:c.3319A>G	NP_002011.2:p.Ile1107Val