Canonical Allele Identifier: CA3606258

Gene: FLT4

Linked Data

• dbSNP Id: rs771777315
• ExAC: 5:180046628 C / CCAG
• gnomAD v2: 5-180046628-C-CCAG
• gnomAD v4: 5-180619628-C-CCAG
• MyVariant Identifiers: chr5:g.180046628_180046629insCAG (hg19) ; chr5:g.180619628_180619629insCAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619630_180619632dup , CM000667.2:g.180619630_180619632dup	GRCh38
NC_000005.9:g.180046630_180046632dup , CM000667.1:g.180046630_180046632dup	GRCh37
NC_000005.8:g.179979236_179979238dup	NCBI36
NG_011536.1:g.34994_34996dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2647+34_2647+36dup MANE Select	ENSP00000261937.6:n.2647+34_2647+36dup
ENST00000261937.10:c.2647+34_2647+36dup	ENSP00000261937.6:n.2647+34_2647+36dup
ENST00000393347.7:c.2647+34_2647+36dup	ENSP00000377016.3:n.2647+34_2647+36dup
ENST00000502649.5:c.2647+34_2647+36dup	ENSP00000426057.1:n.2647+34_2647+36dup
ENST00000507059.5:n.1776_1778dup
ENST00000619105.4:c.*1590+34_*1590+36dup	ENSP00000481134.1:n.*1590+34_*1590+36dup
NM_002020.4:c.2647+34_2647+36dup	NP_002011.2:n.2647+34_2647+36dup
NM_182925.4:c.2647+34_2647+36dup	NP_891555.2:n.2647+34_2647+36dup
XM_011534477.1:c.2896+34_2896+36dup	XP_011532779.1:n.2896+34_2896+36dup
XM_011534478.1:c.2878+34_2878+36dup	XP_011532780.1:n.2878+34_2878+36dup
XM_011534479.1:c.2896+34_2896+36dup	XP_011532781.1:n.2896+34_2896+36dup
XM_011534480.1:c.2896+34_2896+36dup	XP_011532782.1:n.2896+34_2896+36dup
XM_011534481.1:c.2896+34_2896+36dup	XP_011532783.1:n.2896+34_2896+36dup
XM_011534482.1:c.2665+34_2665+36dup	XP_011532784.1:n.2665+34_2665+36dup
XM_011534483.1:c.2587+34_2587+36dup	XP_011532785.1:n.2587+34_2587+36dup
XM_011534484.1:c.2188+34_2188+36dup	XP_011532786.1:n.2188+34_2188+36dup
XR_941095.1:n.2908+34_2908+36dup
NM_001354989.1:c.2647+34_2647+36dup	NP_001341918.1:n.2647+34_2647+36dup
XM_011534478.3:c.2878+34_2878+36dup	XP_011532780.1:n.2878+34_2878+36dup
XM_011534484.2:c.2188+34_2188+36dup	XP_011532786.1:n.2188+34_2188+36dup
XM_017009263.1:c.2878+34_2878+36dup	XP_016864752.1:n.2878+34_2878+36dup
XM_017009264.2:c.2878+34_2878+36dup	XP_016864753.1:n.2878+34_2878+36dup
XM_017009265.1:c.2878+34_2878+36dup	XP_016864754.1:n.2878+34_2878+36dup
XM_017009266.1:c.2878+34_2878+36dup	XP_016864755.1:n.2878+34_2878+36dup
XM_017009267.2:c.2878+34_2878+36dup	XP_016864756.1:n.2878+34_2878+36dup
XM_017009268.1:c.2569+34_2569+36dup	XP_016864757.1:n.2569+34_2569+36dup
XR_001742050.2:n.3112+34_3112+36dup
NM_182925.5:c.2647+34_2647+36dup MANE Select	NP_891555.2:n.2647+34_2647+36dup
NM_001354989.2:c.2647+34_2647+36dup	NP_001341918.1:n.2647+34_2647+36dup
NM_002020.5:c.2647+34_2647+36dup	NP_002011.2:n.2647+34_2647+36dup