Canonical Allele Identifier: CA2616844393

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880730-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880732dup , CM000673.2:g.130880732dup	GRCh38
NC_000011.9:g.130750627dup , CM000673.1:g.130750627dup	GRCh37
NC_000011.8:g.130255837dup	NCBI36
NG_053190.1:g.40758dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2649dup MANE Select	ENSP00000265909.4:p.Ile884HisfsTer9
ENST00000265909.8:c.2649dup	ENSP00000265909.4:p.Ile884HisfsTer9
ENST00000426933.6:c.153dup	ENSP00000413345.2:p.Ile52HisfsTer9
ENST00000526579.5:n.178-1020dup
ENST00000527116.5:n.411dup
ENST00000528555.5:c.789dup	ENSP00000435122.1:p.Ile264HisfsTer9
ENST00000530330.1:n.385dup
ENST00000530356.5:c.789dup	ENSP00000432307.1:p.Ile264HisfsTer9
ENST00000533318.5:n.1009dup
ENST00000534726.5:c.369dup	ENSP00000433699.1:p.Ile124HisfsTer9
NM_001301089.1:c.789dup	NP_001288018.1:p.Ile264HisfsTer9
NM_014758.2:c.2649dup	NP_055573.2:p.Ile884HisfsTer9
XM_005271546.3:c.2574-1020dup	XP_005271603.1:n.2574-1020dup
XM_011542819.1:c.2895dup	XP_011541121.1:p.Ile966HisfsTer9
XM_011542820.1:c.2883dup	XP_011541122.1:p.Ile962HisfsTer9
XM_011542821.1:c.2775dup	XP_011541123.1:p.Ile926HisfsTer9
XM_011542824.1:c.2013dup	XP_011541126.1:p.Ile672HisfsTer9
XM_011542825.1:c.1170dup	XP_011541127.1:p.Ile391HisfsTer9
XM_011542826.1:c.1035dup	XP_011541128.1:p.Ile346HisfsTer9
XM_011542827.1:c.915dup	XP_011541129.1:p.Ile306HisfsTer9
NM_001347918.1:c.2529dup	NP_001334847.1:p.Ile844HisfsTer9
NM_001347919.1:c.2574-1020dup	NP_001334848.1:n.2574-1020dup
NM_001347922.1:c.978dup	NP_001334851.1:p.Ile327HisfsTer9
NM_001347923.1:c.924dup	NP_001334852.1:p.Ile309HisfsTer9
NM_001347924.1:c.669dup	NP_001334853.1:p.Ile224HisfsTer9
NM_001347925.1:c.615dup	NP_001334854.1:p.Ile206HisfsTer9
NM_001347926.1:c.714-1020dup	NP_001334855.1:n.714-1020dup
NM_001347927.1:c.369dup	NP_001334856.1:p.Ile124HisfsTer9
NR_144939.1:n.3282dup
XM_011542820.2:c.2883dup	XP_011541122.1:p.Ile962HisfsTer9
XM_011542821.3:c.2775dup	XP_011541123.1:p.Ile926HisfsTer9
XM_011542824.2:c.2013dup	XP_011541126.1:p.Ile672HisfsTer9
XM_011542825.2:c.1170dup	XP_011541127.1:p.Ile391HisfsTer9
XM_011542826.2:c.1035dup	XP_011541128.1:p.Ile346HisfsTer9
XM_024448521.1:c.2895dup	XP_024304289.1:p.Ile966HisfsTer9
XR_001747870.1:n.3720dup
XR_001747872.1:n.3066dup
XR_001747873.1:n.3380dup
NM_001301089.2:c.789dup	NP_001288018.1:p.Ile264HisfsTer9
NM_001347918.2:c.2529dup	NP_001334847.2:p.Ile844HisfsTer9
NM_001347919.2:c.2574-1020dup	NP_001334848.2:n.2574-1020dup
NM_001347920.2:c.*21045dup	NP_001334849.2:n.*21045dup
NM_001347922.2:c.978dup	NP_001334851.2:p.Ile327HisfsTer9
NM_001347923.2:c.924dup	NP_001334852.2:p.Ile309HisfsTer9
NM_001347924.2:c.669dup	NP_001334853.1:p.Ile224HisfsTer9
NM_001347925.2:c.615dup	NP_001334854.1:p.Ile206HisfsTer9
NM_001347926.2:c.714-1020dup	NP_001334855.1:n.714-1020dup
NM_001347927.2:c.369dup	NP_001334856.1:p.Ile124HisfsTer9
NM_014758.3:c.2649dup MANE Select	NP_055573.3:p.Ile884HisfsTer9
NR_144939.2:n.3274dup