Canonical Allele Identifier: CA2009229689

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880666_130880667delinsGC , CM000673.2:g.130880666_130880667delinsGC	GRCh38
NC_000011.9:g.130750561_130750562delinsGC , CM000673.1:g.130750561_130750562delinsGC	GRCh37
NC_000011.8:g.130255771_130255772delinsGC	NCBI36
NG_053190.1:g.40822_40823delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2713_2714delinsGC MANE Select	ENSP00000265909.4:p.Ala905=
ENST00000265909.8:c.2713_2714delinsGC	ENSP00000265909.4:p.Ala905=
ENST00000426933.6:c.217_218delinsGC	ENSP00000413345.2:p.Ala73=
ENST00000526579.5:n.178-956_178-955delinsGC
ENST00000527116.5:n.475_476delinsGC
ENST00000528555.5:c.853_854delinsGC	ENSP00000435122.1:p.Ala285=
ENST00000530330.1:n.449_450delinsGC
ENST00000530356.5:c.853_854delinsGC	ENSP00000432307.1:p.Ala285=
ENST00000533318.5:n.1073_1074delinsGC
ENST00000534726.5:c.433_434delinsGC	ENSP00000433699.1:p.Ala145=
NM_001301089.1:c.853_854delinsGC	NP_001288018.1:p.Ala285=
NM_014758.2:c.2713_2714delinsGC	NP_055573.2:p.Ala905=
XM_005271546.3:c.2574-956_2574-955delinsGC	XP_005271603.1:n.2574-956_2574-955delinsGC
XM_011542819.1:c.2959_2960delinsGC	XP_011541121.1:p.Ala987=
XM_011542820.1:c.2947_2948delinsGC	XP_011541122.1:p.Ala983=
XM_011542821.1:c.2839_2840delinsGC	XP_011541123.1:p.Ala947=
XM_011542824.1:c.2077_2078delinsGC	XP_011541126.1:p.Ala693=
XM_011542825.1:c.1234_1235delinsGC	XP_011541127.1:p.Ala412=
XM_011542826.1:c.1099_1100delinsGC	XP_011541128.1:p.Ala367=
XM_011542827.1:c.979_980delinsGC	XP_011541129.1:p.Ala327=
NM_001347918.1:c.2593_2594delinsGC	NP_001334847.1:p.Ala865=
NM_001347919.1:c.2574-956_2574-955delinsGC	NP_001334848.1:n.2574-956_2574-955delinsGC
NM_001347922.1:c.1042_1043delinsGC	NP_001334851.1:p.Ala348=
NM_001347923.1:c.988_989delinsGC	NP_001334852.1:p.Ala330=
NM_001347924.1:c.733_734delinsGC	NP_001334853.1:p.Ala245=
NM_001347925.1:c.679_680delinsGC	NP_001334854.1:p.Ala227=
NM_001347926.1:c.714-956_714-955delinsGC	NP_001334855.1:n.714-956_714-955delinsGC
NM_001347927.1:c.433_434delinsGC	NP_001334856.1:p.Ala145=
NR_144939.1:n.3346_3347delinsGC
XM_011542820.2:c.2947_2948delinsGC	XP_011541122.1:p.Ala983=
XM_011542821.3:c.2839_2840delinsGC	XP_011541123.1:p.Ala947=
XM_011542824.2:c.2077_2078delinsGC	XP_011541126.1:p.Ala693=
XM_011542825.2:c.1234_1235delinsGC	XP_011541127.1:p.Ala412=
XM_011542826.2:c.1099_1100delinsGC	XP_011541128.1:p.Ala367=
XM_024448521.1:c.2959_2960delinsGC	XP_024304289.1:p.Ala987=
XR_001747870.1:n.3784_3785delinsGC
XR_001747872.1:n.3130_3131delinsGC
XR_001747873.1:n.3444_3445delinsGC
NM_001301089.2:c.853_854delinsGC	NP_001288018.1:p.Ala285=
NM_001347918.2:c.2593_2594delinsGC	NP_001334847.2:p.Ala865=
NM_001347919.2:c.2574-956_2574-955delinsGC	NP_001334848.2:n.2574-956_2574-955delinsGC
NM_001347920.2:c.*21109_*21110delinsGC	NP_001334849.2:n.*21109_*21110delinsGC
NM_001347922.2:c.1042_1043delinsGC	NP_001334851.2:p.Ala348=
NM_001347923.2:c.988_989delinsGC	NP_001334852.2:p.Ala330=
NM_001347924.2:c.733_734delinsGC	NP_001334853.1:p.Ala245=
NM_001347925.2:c.679_680delinsGC	NP_001334854.1:p.Ala227=
NM_001347926.2:c.714-956_714-955delinsGC	NP_001334855.1:n.714-956_714-955delinsGC
NM_001347927.2:c.433_434delinsGC	NP_001334856.1:p.Ala145=
NM_014758.3:c.2713_2714delinsGC MANE Select	NP_055573.3:p.Ala905=
NR_144939.2:n.3338_3339delinsGC