Canonical Allele Identifier: CA1240248796

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375549G= , CM000664.2:g.27375549G=	GRCh38
NC_000002.11:g.27598416G= , CM000664.1:g.27598416G=	GRCh37
NC_000002.10:g.27451920G=	NCBI36
NG_028219.1:g.10196C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.818G= MANE Select	ENSP00000233575.2:p.Arg273=
ENST00000233575.6:c.818G=	ENSP00000233575.2:p.Arg273=
ENST00000427123.5:c.*628G=	ENSP00000405399.1:n.*628G=
ENST00000440760.5:c.*663G=	ENSP00000399727.1:n.*663G=
ENST00000453453.1:c.*345G=	ENSP00000401922.1:n.*345G=
ENST00000493711.1:n.535G=
ENST00000537606.5:c.743G=	ENSP00000439208.1:p.Arg248=
NM_001267059.1:c.782G=	NP_001253988.1:p.Arg261=
NM_001267060.1:c.743G=	NP_001253989.1:p.Arg248=
NM_001267061.1:c.758G=	NP_001253990.1:p.Arg253=
NM_014748.3:c.818G=	NP_055563.1:p.Arg273=
NR_049782.1:n.1191G=
NR_049783.1:n.1164G=
NR_049784.1:n.1140G=
NR_049785.1:n.1073G=
NR_049786.1:n.1022G=
NR_049787.1:n.873G=
NR_049788.1:n.803G=
XM_011533203.1:c.176G=	XP_011531505.1:p.Arg59=
XM_011533203.2:c.176G=	XP_011531505.1:p.Arg59=
XM_017005405.2:c.176G=	XP_016860894.1:p.Arg59=
NM_014748.4:c.818G= MANE Select	NP_055563.1:p.Arg273=
NM_001267059.2:c.782G=	NP_001253988.1:p.Arg261=
NM_001267061.2:c.758G=	NP_001253990.1:p.Arg253=
NR_049782.2:n.1071G=
NR_049783.2:n.1044G=
NR_049784.2:n.1020G=
NR_049785.2:n.953G=
NR_049786.2:n.902G=
NR_049787.2:n.753G=
NR_049788.2:n.683G=
NM_001267060.2:c.743G=	NP_001253989.1:p.Arg248=