Canonical Allele Identifier: CA1240248693

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375513G= , CM000664.2:g.27375513G=	GRCh38
NC_000002.11:g.27598380G= , CM000664.1:g.27598380G=	GRCh37
NC_000002.10:g.27451884G=	NCBI36
NG_028219.1:g.10232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.782G= MANE Select	ENSP00000233575.2:p.Arg261=
ENST00000233575.6:c.782G=	ENSP00000233575.2:p.Arg261=
ENST00000427123.5:c.*592G=	ENSP00000405399.1:n.*592G=
ENST00000440760.5:c.*627G=	ENSP00000399727.1:n.*627G=
ENST00000453453.1:c.*309G=	ENSP00000401922.1:n.*309G=
ENST00000493711.1:n.499G=
ENST00000494893.5:n.958G=
ENST00000537606.5:c.707G=	ENSP00000439208.1:p.Arg236=
NM_001267059.1:c.746G=	NP_001253988.1:p.Arg249=
NM_001267060.1:c.707G=	NP_001253989.1:p.Arg236=
NM_001267061.1:c.722G=	NP_001253990.1:p.Arg241=
NM_014748.3:c.782G=	NP_055563.1:p.Arg261=
NR_049782.1:n.1155G=
NR_049783.1:n.1128G=
NR_049784.1:n.1104G=
NR_049785.1:n.1037G=
NR_049786.1:n.986G=
NR_049787.1:n.837G=
NR_049788.1:n.767G=
XM_011533203.1:c.140G=	XP_011531505.1:p.Arg47=
XM_011533203.2:c.140G=	XP_011531505.1:p.Arg47=
XM_017005405.2:c.140G=	XP_016860894.1:p.Arg47=
NM_014748.4:c.782G= MANE Select	NP_055563.1:p.Arg261=
NM_001267059.2:c.746G=	NP_001253988.1:p.Arg249=
NM_001267061.2:c.722G=	NP_001253990.1:p.Arg241=
NR_049782.2:n.1035G=
NR_049783.2:n.1008G=
NR_049784.2:n.984G=
NR_049785.2:n.917G=
NR_049786.2:n.866G=
NR_049787.2:n.717G=
NR_049788.2:n.647G=
NM_001267060.2:c.707G=	NP_001253989.1:p.Arg236=