Canonical Allele Identifier: CA3606190

Gene: FLT4

Linked Data

• dbSNP Id: rs1554112082
• ExAC: 5:180046423 C / CTACTGGCCGCTTAGCTAAGG
• gnomAD v2: 5-180046423-C-CTACTGGCCGCTTAGCTAAGG
• gnomAD v4: 5-180619423-C-CTACTGGCCGCTTAGCTAAGG
• MyVariant Identifiers: chr5:g.180046423_180046424insTACTGGCCGCTTAGCTAAGG (hg19) ; chr5:g.180619423_180619424insTACTGGCCGCTTAGCTAAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619423_180619424insTACTGGCCGCTTAGCTAAGG , CM000667.2:g.180619423_180619424insTACTGGCCGCTTAGCTAAGG	GRCh38
NC_000005.9:g.180046423_180046424insTACTGGCCGCTTAGCTAAGG , CM000667.1:g.180046423_180046424insTACTGGCCGCTTAGCTAAGG	GRCh37
NC_000005.8:g.179979029_179979030insTACTGGCCGCTTAGCTAAGG	NCBI36
NG_011536.1:g.35201_35202insCCTTAGCTAAGCGGCCAGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA MANE Select	ENSP00000261937.6:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
ENST00000261937.10:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	ENSP00000261937.6:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
ENST00000393347.7:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	ENSP00000377016.3:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
ENST00000502649.5:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	ENSP00000426057.1:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
ENST00000507059.5:n.1983_1984insCCTTAGCTAAGCGGCCAGTA
ENST00000619105.4:c.*1591-58_*1591-57insCCTTAGCTAAGCGGCCAGTA	ENSP00000481134.1:n.*1591-58_*1591-57insCCTTAGCTAAGCGGCCAGTA
NM_002020.4:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	NP_002011.2:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
NM_182925.4:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	NP_891555.2:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
XM_011534477.1:c.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA	XP_011532779.1:n.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA
XM_011534478.1:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_011532780.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_011534479.1:c.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA	XP_011532781.1:n.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA
XM_011534480.1:c.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA	XP_011532782.1:n.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA
XM_011534481.1:c.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA	XP_011532783.1:n.2897-58_2897-57insCCTTAGCTAAGCGGCCAGTA
XM_011534482.1:c.2666-58_2666-57insCCTTAGCTAAGCGGCCAGTA	XP_011532784.1:n.2666-58_2666-57insCCTTAGCTAAGCGGCCAGTA
XM_011534483.1:c.2588-58_2588-57insCCTTAGCTAAGCGGCCAGTA	XP_011532785.1:n.2588-58_2588-57insCCTTAGCTAAGCGGCCAGTA
XM_011534484.1:c.2189-58_2189-57insCCTTAGCTAAGCGGCCAGTA	XP_011532786.1:n.2189-58_2189-57insCCTTAGCTAAGCGGCCAGTA
XR_941095.1:n.2909-58_2909-57insCCTTAGCTAAGCGGCCAGTA
NM_001354989.1:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	NP_001341918.1:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
XM_011534478.3:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_011532780.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_011534484.2:c.2189-58_2189-57insCCTTAGCTAAGCGGCCAGTA	XP_011532786.1:n.2189-58_2189-57insCCTTAGCTAAGCGGCCAGTA
XM_017009263.1:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_016864752.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_017009264.2:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_016864753.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_017009265.1:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_016864754.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_017009266.1:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_016864755.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_017009267.2:c.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA	XP_016864756.1:n.2879-58_2879-57insCCTTAGCTAAGCGGCCAGTA
XM_017009268.1:c.2570-58_2570-57insCCTTAGCTAAGCGGCCAGTA	XP_016864757.1:n.2570-58_2570-57insCCTTAGCTAAGCGGCCAGTA
XR_001742050.2:n.3113-58_3113-57insCCTTAGCTAAGCGGCCAGTA
NM_182925.5:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA MANE Select	NP_891555.2:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
NM_001354989.2:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	NP_001341918.1:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA
NM_002020.5:c.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA	NP_002011.2:n.2648-58_2648-57insCCTTAGCTAAGCGGCCAGTA