Canonical Allele Identifier: CA1240248684

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375512A= , CM000664.2:g.27375512A=	GRCh38
NC_000002.11:g.27598379A= , CM000664.1:g.27598379A=	GRCh37
NC_000002.10:g.27451883A=	NCBI36
NG_028219.1:g.10233T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.781A= MANE Select	ENSP00000233575.2:p.Arg261=
ENST00000233575.6:c.781A=	ENSP00000233575.2:p.Arg261=
ENST00000427123.5:c.*591A=	ENSP00000405399.1:n.*591A=
ENST00000440760.5:c.*626A=	ENSP00000399727.1:n.*626A=
ENST00000453453.1:c.*308A=	ENSP00000401922.1:n.*308A=
ENST00000493711.1:n.498A=
ENST00000494893.5:n.957A=
ENST00000537606.5:c.706A=	ENSP00000439208.1:p.Arg236=
NM_001267059.1:c.745A=	NP_001253988.1:p.Arg249=
NM_001267060.1:c.706A=	NP_001253989.1:p.Arg236=
NM_001267061.1:c.721A=	NP_001253990.1:p.Arg241=
NM_014748.3:c.781A=	NP_055563.1:p.Arg261=
NR_049782.1:n.1154A=
NR_049783.1:n.1127A=
NR_049784.1:n.1103A=
NR_049785.1:n.1036A=
NR_049786.1:n.985A=
NR_049787.1:n.836A=
NR_049788.1:n.766A=
XM_011533203.1:c.139A=	XP_011531505.1:p.Arg47=
XM_011533203.2:c.139A=	XP_011531505.1:p.Arg47=
XM_017005405.2:c.139A=	XP_016860894.1:p.Arg47=
NM_014748.4:c.781A= MANE Select	NP_055563.1:p.Arg261=
NM_001267059.2:c.745A=	NP_001253988.1:p.Arg249=
NM_001267061.2:c.721A=	NP_001253990.1:p.Arg241=
NR_049782.2:n.1034A=
NR_049783.2:n.1007A=
NR_049784.2:n.983A=
NR_049785.2:n.916A=
NR_049786.2:n.865A=
NR_049787.2:n.716A=
NR_049788.2:n.646A=
NM_001267060.2:c.706A=	NP_001253989.1:p.Arg236=