Canonical Allele Identifier: CA362501855

Gene: FLT4

Linked Data

• gnomAD v4: 5-180619751-C-T
• MyVariant Identifiers: chr5:g.180046751C>T (hg19) ; chr5:g.180619751C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619751C>T , CM000667.2:g.180619751C>T	GRCh38
NC_000005.9:g.180046751C>T , CM000667.1:g.180046751C>T	GRCh37
NC_000005.8:g.179979357C>T	NCBI36
NG_011536.1:g.34874G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.2561G>A MANE Select	ENSP00000261937.6:p.Gly854Asp
ENST00000261937.10:c.2561G>A	ENSP00000261937.6:p.Gly854Asp
ENST00000393347.7:c.2561G>A	ENSP00000377016.3:p.Gly854Asp
ENST00000502649.5:c.2561G>A	ENSP00000426057.1:p.Gly854Asp
ENST00000507059.5:n.1656G>A
ENST00000619105.4:c.*1504G>A	ENSP00000481134.1:n.*1504G>A
NM_002020.4:c.2561G>A	NP_002011.2:p.Gly854Asp
NM_182925.4:c.2561G>A	NP_891555.2:p.Gly854Asp
XM_011534477.1:c.2810G>A	XP_011532779.1:p.Gly937Asp
XM_011534478.1:c.2792G>A	XP_011532780.1:p.Gly931Asp
XM_011534479.1:c.2810G>A	XP_011532781.1:p.Gly937Asp
XM_011534480.1:c.2810G>A	XP_011532782.1:p.Gly937Asp
XM_011534481.1:c.2810G>A	XP_011532783.1:p.Gly937Asp
XM_011534482.1:c.2579G>A	XP_011532784.1:p.Gly860Asp
XM_011534483.1:c.2501G>A	XP_011532785.1:p.Gly834Asp
XM_011534484.1:c.2102G>A	XP_011532786.1:p.Gly701Asp
XR_941095.1:n.2822G>A
NM_001354989.1:c.2561G>A	NP_001341918.1:p.Gly854Asp
XM_011534478.3:c.2792G>A	XP_011532780.1:p.Gly931Asp
XM_011534484.2:c.2102G>A	XP_011532786.1:p.Gly701Asp
XM_017009263.1:c.2792G>A	XP_016864752.1:p.Gly931Asp
XM_017009264.2:c.2792G>A	XP_016864753.1:p.Gly931Asp
XM_017009265.1:c.2792G>A	XP_016864754.1:p.Gly931Asp
XM_017009266.1:c.2792G>A	XP_016864755.1:p.Gly931Asp
XM_017009267.2:c.2792G>A	XP_016864756.1:p.Gly931Asp
XM_017009268.1:c.2483G>A	XP_016864757.1:p.Gly828Asp
XR_001742050.2:n.3026G>A
NM_182925.5:c.2561G>A MANE Select	NP_891555.2:p.Gly854Asp
NM_001354989.2:c.2561G>A	NP_001341918.1:p.Gly854Asp
NM_002020.5:c.2561G>A	NP_002011.2:p.Gly854Asp