Canonical Allele Identifier: CA3606247

Gene: FLT4

Linked Data

• dbSNP Id: rs745911364
• ExAC: 5:180046571 TCA / T
• gnomAD v2: 5-180046571-TCA-T
• gnomAD v3: 5-180619571-TCA-T
• gnomAD v4: 5-180619571-TCA-T
• MyVariant Identifiers: chr5:g.180046572_180046573del (hg19) ; chr5:g.180619572_180619573del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619572_180619573del , CM000667.2:g.180619572_180619573del	GRCh38
NC_000005.9:g.180046572_180046573del , CM000667.1:g.180046572_180046573del	GRCh37
NC_000005.8:g.179979178_179979179del	NCBI36
NG_011536.1:g.35052_35053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2647+92_2647+93del MANE Select	ENSP00000261937.6:n.2647+92_2647+93del
ENST00000261937.10:c.2647+92_2647+93del	ENSP00000261937.6:n.2647+92_2647+93del
ENST00000393347.7:c.2647+92_2647+93del	ENSP00000377016.3:n.2647+92_2647+93del
ENST00000502649.5:c.2647+92_2647+93del	ENSP00000426057.1:n.2647+92_2647+93del
ENST00000507059.5:n.1834_1835del
ENST00000619105.4:c.*1590+92_*1590+93del	ENSP00000481134.1:n.*1590+92_*1590+93del
NM_002020.4:c.2647+92_2647+93del	NP_002011.2:n.2647+92_2647+93del
NM_182925.4:c.2647+92_2647+93del	NP_891555.2:n.2647+92_2647+93del
XM_011534477.1:c.2896+92_2896+93del	XP_011532779.1:n.2896+92_2896+93del
XM_011534478.1:c.2878+92_2878+93del	XP_011532780.1:n.2878+92_2878+93del
XM_011534479.1:c.2896+92_2896+93del	XP_011532781.1:n.2896+92_2896+93del
XM_011534480.1:c.2896+92_2896+93del	XP_011532782.1:n.2896+92_2896+93del
XM_011534481.1:c.2896+92_2896+93del	XP_011532783.1:n.2896+92_2896+93del
XM_011534482.1:c.2665+92_2665+93del	XP_011532784.1:n.2665+92_2665+93del
XM_011534483.1:c.2587+92_2587+93del	XP_011532785.1:n.2587+92_2587+93del
XM_011534484.1:c.2188+92_2188+93del	XP_011532786.1:n.2188+92_2188+93del
XR_941095.1:n.2908+92_2908+93del
NM_001354989.1:c.2647+92_2647+93del	NP_001341918.1:n.2647+92_2647+93del
XM_011534478.3:c.2878+92_2878+93del	XP_011532780.1:n.2878+92_2878+93del
XM_011534484.2:c.2188+92_2188+93del	XP_011532786.1:n.2188+92_2188+93del
XM_017009263.1:c.2878+92_2878+93del	XP_016864752.1:n.2878+92_2878+93del
XM_017009264.2:c.2878+92_2878+93del	XP_016864753.1:n.2878+92_2878+93del
XM_017009265.1:c.2878+92_2878+93del	XP_016864754.1:n.2878+92_2878+93del
XM_017009266.1:c.2878+92_2878+93del	XP_016864755.1:n.2878+92_2878+93del
XM_017009267.2:c.2878+92_2878+93del	XP_016864756.1:n.2878+92_2878+93del
XM_017009268.1:c.2569+92_2569+93del	XP_016864757.1:n.2569+92_2569+93del
XR_001742050.2:n.3112+92_3112+93del
NM_182925.5:c.2647+92_2647+93del MANE Select	NP_891555.2:n.2647+92_2647+93del
NM_001354989.2:c.2647+92_2647+93del	NP_001341918.1:n.2647+92_2647+93del
NM_002020.5:c.2647+92_2647+93del	NP_002011.2:n.2647+92_2647+93del