Canonical Allele Identifier: CA1240248793

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375548C= , CM000664.2:g.27375548C=	GRCh38
NC_000002.11:g.27598415C= , CM000664.1:g.27598415C=	GRCh37
NC_000002.10:g.27451919C=	NCBI36
NG_028219.1:g.10197G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.817C= MANE Select	ENSP00000233575.2:p.Arg273=
ENST00000233575.6:c.817C=	ENSP00000233575.2:p.Arg273=
ENST00000427123.5:c.*627C=	ENSP00000405399.1:n.*627C=
ENST00000440760.5:c.*662C=	ENSP00000399727.1:n.*662C=
ENST00000453453.1:c.*344C=	ENSP00000401922.1:n.*344C=
ENST00000493711.1:n.534C=
ENST00000537606.5:c.742C=	ENSP00000439208.1:p.Arg248=
NM_001267059.1:c.781C=	NP_001253988.1:p.Arg261=
NM_001267060.1:c.742C=	NP_001253989.1:p.Arg248=
NM_001267061.1:c.757C=	NP_001253990.1:p.Arg253=
NM_014748.3:c.817C=	NP_055563.1:p.Arg273=
NR_049782.1:n.1190C=
NR_049783.1:n.1163C=
NR_049784.1:n.1139C=
NR_049785.1:n.1072C=
NR_049786.1:n.1021C=
NR_049787.1:n.872C=
NR_049788.1:n.802C=
XM_011533203.1:c.175C=	XP_011531505.1:p.Arg59=
XM_011533203.2:c.175C=	XP_011531505.1:p.Arg59=
XM_017005405.2:c.175C=	XP_016860894.1:p.Arg59=
NM_014748.4:c.817C= MANE Select	NP_055563.1:p.Arg273=
NM_001267059.2:c.781C=	NP_001253988.1:p.Arg261=
NM_001267061.2:c.757C=	NP_001253990.1:p.Arg253=
NR_049782.2:n.1070C=
NR_049783.2:n.1043C=
NR_049784.2:n.1019C=
NR_049785.2:n.952C=
NR_049786.2:n.901C=
NR_049787.2:n.752C=
NR_049788.2:n.682C=
NM_001267060.2:c.742C=	NP_001253989.1:p.Arg248=