Canonical Allele Identifier: CA2009229807

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880733_130880736delinsACTC , CM000673.2:g.130880733_130880736delinsACTC	GRCh38
NC_000011.9:g.130750628_130750631delinsACTC , CM000673.1:g.130750628_130750631delinsACTC	GRCh37
NC_000011.8:g.130255838_130255841delinsACTC	NCBI36
NG_053190.1:g.40753_40756delinsGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2644_2647delinsGAGT MANE Select	ENSP00000265909.4:p.Glu882=
ENST00000265909.8:c.2644_2647delinsGAGT	ENSP00000265909.4:p.Glu882=
ENST00000426933.6:c.148_151delinsGAGT	ENSP00000413345.2:p.Glu50=
ENST00000526579.5:n.178-1025_178-1022delinsGAGT
ENST00000527116.5:n.406_409delinsGAGT
ENST00000528555.5:c.784_787delinsGAGT	ENSP00000435122.1:p.Glu262=
ENST00000530330.1:n.380_383delinsGAGT
ENST00000530356.5:c.784_787delinsGAGT	ENSP00000432307.1:p.Glu262=
ENST00000533318.5:n.1004_1007delinsGAGT
ENST00000534726.5:c.364_367delinsGAGT	ENSP00000433699.1:p.Glu122=
NM_001301089.1:c.784_787delinsGAGT	NP_001288018.1:p.Glu262=
NM_014758.2:c.2644_2647delinsGAGT	NP_055573.2:p.Glu882=
XM_005271546.3:c.2574-1025_2574-1022delinsGAGT	XP_005271603.1:n.2574-1025_2574-1022delinsGAGT
XM_011542819.1:c.2890_2893delinsGAGT	XP_011541121.1:p.Glu964=
XM_011542820.1:c.2878_2881delinsGAGT	XP_011541122.1:p.Glu960=
XM_011542821.1:c.2770_2773delinsGAGT	XP_011541123.1:p.Glu924=
XM_011542824.1:c.2008_2011delinsGAGT	XP_011541126.1:p.Glu670=
XM_011542825.1:c.1165_1168delinsGAGT	XP_011541127.1:p.Glu389=
XM_011542826.1:c.1030_1033delinsGAGT	XP_011541128.1:p.Glu344=
XM_011542827.1:c.910_913delinsGAGT	XP_011541129.1:p.Glu304=
NM_001347918.1:c.2524_2527delinsGAGT	NP_001334847.1:p.Glu842=
NM_001347919.1:c.2574-1025_2574-1022delinsGAGT	NP_001334848.1:n.2574-1025_2574-1022delinsGAGT
NM_001347922.1:c.973_976delinsGAGT	NP_001334851.1:p.Glu325=
NM_001347923.1:c.919_922delinsGAGT	NP_001334852.1:p.Glu307=
NM_001347924.1:c.664_667delinsGAGT	NP_001334853.1:p.Glu222=
NM_001347925.1:c.610_613delinsGAGT	NP_001334854.1:p.Glu204=
NM_001347926.1:c.714-1025_714-1022delinsGAGT	NP_001334855.1:n.714-1025_714-1022delinsGAGT
NM_001347927.1:c.364_367delinsGAGT	NP_001334856.1:p.Glu122=
NR_144939.1:n.3277_3280delinsGAGT
XM_011542820.2:c.2878_2881delinsGAGT	XP_011541122.1:p.Glu960=
XM_011542821.3:c.2770_2773delinsGAGT	XP_011541123.1:p.Glu924=
XM_011542824.2:c.2008_2011delinsGAGT	XP_011541126.1:p.Glu670=
XM_011542825.2:c.1165_1168delinsGAGT	XP_011541127.1:p.Glu389=
XM_011542826.2:c.1030_1033delinsGAGT	XP_011541128.1:p.Glu344=
XM_024448521.1:c.2890_2893delinsGAGT	XP_024304289.1:p.Glu964=
XR_001747870.1:n.3715_3718delinsGAGT
XR_001747872.1:n.3061_3064delinsGAGT
XR_001747873.1:n.3375_3378delinsGAGT
NM_001301089.2:c.784_787delinsGAGT	NP_001288018.1:p.Glu262=
NM_001347918.2:c.2524_2527delinsGAGT	NP_001334847.2:p.Glu842=
NM_001347919.2:c.2574-1025_2574-1022delinsGAGT	NP_001334848.2:n.2574-1025_2574-1022delinsGAGT
NM_001347920.2:c.*21040_*21043delinsGAGT	NP_001334849.2:n.*21040_*21043delinsGAGT
NM_001347922.2:c.973_976delinsGAGT	NP_001334851.2:p.Glu325=
NM_001347923.2:c.919_922delinsGAGT	NP_001334852.2:p.Glu307=
NM_001347924.2:c.664_667delinsGAGT	NP_001334853.1:p.Glu222=
NM_001347925.2:c.610_613delinsGAGT	NP_001334854.1:p.Glu204=
NM_001347926.2:c.714-1025_714-1022delinsGAGT	NP_001334855.1:n.714-1025_714-1022delinsGAGT
NM_001347927.2:c.364_367delinsGAGT	NP_001334856.1:p.Glu122=
NM_014758.3:c.2644_2647delinsGAGT MANE Select	NP_055573.3:p.Glu882=
NR_144939.2:n.3269_3272delinsGAGT