Canonical Allele Identifier: CA2009229731

Gene: SNX19

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880687C= , CM000673.2:g.130880687C=	GRCh38
NC_000011.9:g.130750582C= , CM000673.1:g.130750582C=	GRCh37
NC_000011.8:g.130255792C=	NCBI36
NG_053190.1:g.40802G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2693G= MANE Select	ENSP00000265909.4:p.Arg898=
ENST00000265909.8:c.2693G=	ENSP00000265909.4:p.Arg898=
ENST00000426933.6:c.197G=	ENSP00000413345.2:p.Arg66=
ENST00000526579.5:n.178-976G=
ENST00000527116.5:n.455G=
ENST00000528555.5:c.833G=	ENSP00000435122.1:p.Arg278=
ENST00000530330.1:n.429G=
ENST00000530356.5:c.833G=	ENSP00000432307.1:p.Arg278=
ENST00000533318.5:n.1053G=
ENST00000534726.5:c.413G=	ENSP00000433699.1:p.Arg138=
NM_001301089.1:c.833G=	NP_001288018.1:p.Arg278=
NM_014758.2:c.2693G=	NP_055573.2:p.Arg898=
XM_005271546.3:c.2574-976G=	XP_005271603.1:n.2574-976G=
XM_011542819.1:c.2939G=	XP_011541121.1:p.Arg980=
XM_011542820.1:c.2927G=	XP_011541122.1:p.Arg976=
XM_011542821.1:c.2819G=	XP_011541123.1:p.Arg940=
XM_011542824.1:c.2057G=	XP_011541126.1:p.Arg686=
XM_011542825.1:c.1214G=	XP_011541127.1:p.Arg405=
XM_011542826.1:c.1079G=	XP_011541128.1:p.Arg360=
XM_011542827.1:c.959G=	XP_011541129.1:p.Arg320=
NM_001347918.1:c.2573G=	NP_001334847.1:p.Arg858=
NM_001347919.1:c.2574-976G=	NP_001334848.1:n.2574-976G=
NM_001347922.1:c.1022G=	NP_001334851.1:p.Arg341=
NM_001347923.1:c.968G=	NP_001334852.1:p.Arg323=
NM_001347924.1:c.713G=	NP_001334853.1:p.Arg238=
NM_001347925.1:c.659G=	NP_001334854.1:p.Arg220=
NM_001347926.1:c.714-976G=	NP_001334855.1:n.714-976G=
NM_001347927.1:c.413G=	NP_001334856.1:p.Arg138=
NR_144939.1:n.3326G=
XM_011542820.2:c.2927G=	XP_011541122.1:p.Arg976=
XM_011542821.3:c.2819G=	XP_011541123.1:p.Arg940=
XM_011542824.2:c.2057G=	XP_011541126.1:p.Arg686=
XM_011542825.2:c.1214G=	XP_011541127.1:p.Arg405=
XM_011542826.2:c.1079G=	XP_011541128.1:p.Arg360=
XM_024448521.1:c.2939G=	XP_024304289.1:p.Arg980=
XR_001747870.1:n.3764G=
XR_001747872.1:n.3110G=
XR_001747873.1:n.3424G=
NM_001301089.2:c.833G=	NP_001288018.1:p.Arg278=
NM_001347918.2:c.2573G=	NP_001334847.2:p.Arg858=
NM_001347919.2:c.2574-976G=	NP_001334848.2:n.2574-976G=
NM_001347920.2:c.*21089G=	NP_001334849.2:n.*21089G=
NM_001347922.2:c.1022G=	NP_001334851.2:p.Arg341=
NM_001347923.2:c.968G=	NP_001334852.2:p.Arg323=
NM_001347924.2:c.713G=	NP_001334853.1:p.Arg238=
NM_001347925.2:c.659G=	NP_001334854.1:p.Arg220=
NM_001347926.2:c.714-976G=	NP_001334855.1:n.714-976G=
NM_001347927.2:c.413G=	NP_001334856.1:p.Arg138=
NM_014758.3:c.2693G= MANE Select	NP_055573.3:p.Arg898=
NR_144939.2:n.3318G=