Canonical Allele Identifier: CA1240248013

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375099C= , CM000664.2:g.27375099C=	GRCh38
NC_000002.11:g.27597966C= , CM000664.1:g.27597966C=	GRCh37
NC_000002.10:g.27451470C=	NCBI36
NG_009305.1:g.359G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.720C= MANE Select	ENSP00000233575.2:p.Thr240=
ENST00000233575.6:c.720C=	ENSP00000233575.2:p.Thr240=
ENST00000427123.5:c.*530C=	ENSP00000405399.1:n.*530C=
ENST00000440760.5:c.*565C=	ENSP00000399727.1:n.*565C=
ENST00000453453.1:c.*247C=	ENSP00000401922.1:n.*247C=
ENST00000493711.1:n.437C=
ENST00000494893.5:n.896C=
ENST00000537606.5:c.645C=	ENSP00000439208.1:p.Thr215=
NM_001267059.1:c.684C=	NP_001253988.1:p.Thr228=
NM_001267060.1:c.645C=	NP_001253989.1:p.Thr215=
NM_001267061.1:c.660C=	NP_001253990.1:p.Thr220=
NM_014748.3:c.720C=	NP_055563.1:p.Thr240=
NR_049782.1:n.1093C=
NR_049783.1:n.1066C=
NR_049784.1:n.1042C=
NR_049785.1:n.975C=
NR_049786.1:n.924C=
NR_049787.1:n.775C=
NR_049788.1:n.705C=
XM_011533203.1:c.78C=	XP_011531505.1:p.Thr26=
XM_011533203.2:c.78C=	XP_011531505.1:p.Thr26=
XM_017005405.2:c.78C=	XP_016860894.1:p.Thr26=
NM_014748.4:c.720C= MANE Select	NP_055563.1:p.Thr240=
NM_001267059.2:c.684C=	NP_001253988.1:p.Thr228=
NM_001267061.2:c.660C=	NP_001253990.1:p.Thr220=
NR_049782.2:n.973C=
NR_049783.2:n.946C=
NR_049784.2:n.922C=
NR_049785.2:n.855C=
NR_049786.2:n.804C=
NR_049787.2:n.655C=
NR_049788.2:n.585C=
NM_001267060.2:c.645C=	NP_001253989.1:p.Thr215=