Canonical Allele Identifier: CA2616844392

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880727-A-AGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880729_130880731dup , CM000673.2:g.130880729_130880731dup	GRCh38
NC_000011.9:g.130750624_130750626dup , CM000673.1:g.130750624_130750626dup	GRCh37
NC_000011.8:g.130255834_130255836dup	NCBI36
NG_053190.1:g.40759_40761dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2650_2652dup MANE Select	ENSP00000265909.4:p.Ile884_Trp885insIle
ENST00000265909.8:c.2650_2652dup	ENSP00000265909.4:p.Ile884_Trp885insIle
ENST00000426933.6:c.154_156dup	ENSP00000413345.2:p.Ile52_Trp53insIle
ENST00000526579.5:n.178-1019_178-1017dup
ENST00000527116.5:n.412_414dup
ENST00000528555.5:c.790_792dup	ENSP00000435122.1:p.Ile264_Trp265insIle
ENST00000530330.1:n.386_388dup
ENST00000530356.5:c.790_792dup	ENSP00000432307.1:p.Ile264_Trp265insIle
ENST00000533318.5:n.1010_1012dup
ENST00000534726.5:c.370_372dup	ENSP00000433699.1:p.Ile124_Trp125insIle
NM_001301089.1:c.790_792dup	NP_001288018.1:p.Ile264_Trp265insIle
NM_014758.2:c.2650_2652dup	NP_055573.2:p.Ile884_Trp885insIle
XM_005271546.3:c.2574-1019_2574-1017dup	XP_005271603.1:n.2574-1019_2574-1017dup
XM_011542819.1:c.2896_2898dup	XP_011541121.1:p.Ile966_Trp967insIle
XM_011542820.1:c.2884_2886dup	XP_011541122.1:p.Ile962_Trp963insIle
XM_011542821.1:c.2776_2778dup	XP_011541123.1:p.Ile926_Trp927insIle
XM_011542824.1:c.2014_2016dup	XP_011541126.1:p.Ile672_Trp673insIle
XM_011542825.1:c.1171_1173dup	XP_011541127.1:p.Ile391_Trp392insIle
XM_011542826.1:c.1036_1038dup	XP_011541128.1:p.Ile346_Trp347insIle
XM_011542827.1:c.916_918dup	XP_011541129.1:p.Ile306_Trp307insIle
NM_001347918.1:c.2530_2532dup	NP_001334847.1:p.Ile844_Trp845insIle
NM_001347919.1:c.2574-1019_2574-1017dup	NP_001334848.1:n.2574-1019_2574-1017dup
NM_001347922.1:c.979_981dup	NP_001334851.1:p.Ile327_Trp328insIle
NM_001347923.1:c.925_927dup	NP_001334852.1:p.Ile309_Trp310insIle
NM_001347924.1:c.670_672dup	NP_001334853.1:p.Ile224_Trp225insIle
NM_001347925.1:c.616_618dup	NP_001334854.1:p.Ile206_Trp207insIle
NM_001347926.1:c.714-1019_714-1017dup	NP_001334855.1:n.714-1019_714-1017dup
NM_001347927.1:c.370_372dup	NP_001334856.1:p.Ile124_Trp125insIle
NR_144939.1:n.3283_3285dup
XM_011542820.2:c.2884_2886dup	XP_011541122.1:p.Ile962_Trp963insIle
XM_011542821.3:c.2776_2778dup	XP_011541123.1:p.Ile926_Trp927insIle
XM_011542824.2:c.2014_2016dup	XP_011541126.1:p.Ile672_Trp673insIle
XM_011542825.2:c.1171_1173dup	XP_011541127.1:p.Ile391_Trp392insIle
XM_011542826.2:c.1036_1038dup	XP_011541128.1:p.Ile346_Trp347insIle
XM_024448521.1:c.2896_2898dup	XP_024304289.1:p.Ile966_Trp967insIle
XR_001747870.1:n.3721_3723dup
XR_001747872.1:n.3067_3069dup
XR_001747873.1:n.3381_3383dup
NM_001301089.2:c.790_792dup	NP_001288018.1:p.Ile264_Trp265insIle
NM_001347918.2:c.2530_2532dup	NP_001334847.2:p.Ile844_Trp845insIle
NM_001347919.2:c.2574-1019_2574-1017dup	NP_001334848.2:n.2574-1019_2574-1017dup
NM_001347920.2:c.*21046_*21048dup	NP_001334849.2:n.*21046_*21048dup
NM_001347922.2:c.979_981dup	NP_001334851.2:p.Ile327_Trp328insIle
NM_001347923.2:c.925_927dup	NP_001334852.2:p.Ile309_Trp310insIle
NM_001347924.2:c.670_672dup	NP_001334853.1:p.Ile224_Trp225insIle
NM_001347925.2:c.616_618dup	NP_001334854.1:p.Ile206_Trp207insIle
NM_001347926.2:c.714-1019_714-1017dup	NP_001334855.1:n.714-1019_714-1017dup
NM_001347927.2:c.370_372dup	NP_001334856.1:p.Ile124_Trp125insIle
NM_014758.3:c.2650_2652dup MANE Select	NP_055573.3:p.Ile884_Trp885insIle
NR_144939.2:n.3275_3277dup