Canonical Allele Identifier: CA1240248712

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375526G= , CM000664.2:g.27375526G=	GRCh38
NC_000002.11:g.27598393G= , CM000664.1:g.27598393G=	GRCh37
NC_000002.10:g.27451897G=	NCBI36
NG_028219.1:g.10219C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.795G= MANE Select	ENSP00000233575.2:p.Thr265=
ENST00000233575.6:c.795G=	ENSP00000233575.2:p.Thr265=
ENST00000427123.5:c.*605G=	ENSP00000405399.1:n.*605G=
ENST00000440760.5:c.*640G=	ENSP00000399727.1:n.*640G=
ENST00000453453.1:c.*322G=	ENSP00000401922.1:n.*322G=
ENST00000493711.1:n.512G=
ENST00000537606.5:c.720G=	ENSP00000439208.1:p.Thr240=
NM_001267059.1:c.759G=	NP_001253988.1:p.Thr253=
NM_001267060.1:c.720G=	NP_001253989.1:p.Thr240=
NM_001267061.1:c.735G=	NP_001253990.1:p.Thr245=
NM_014748.3:c.795G=	NP_055563.1:p.Thr265=
NR_049782.1:n.1168G=
NR_049783.1:n.1141G=
NR_049784.1:n.1117G=
NR_049785.1:n.1050G=
NR_049786.1:n.999G=
NR_049787.1:n.850G=
NR_049788.1:n.780G=
XM_011533203.1:c.153G=	XP_011531505.1:p.Thr51=
XM_011533203.2:c.153G=	XP_011531505.1:p.Thr51=
XM_017005405.2:c.153G=	XP_016860894.1:p.Thr51=
NM_014748.4:c.795G= MANE Select	NP_055563.1:p.Thr265=
NM_001267059.2:c.759G=	NP_001253988.1:p.Thr253=
NM_001267061.2:c.735G=	NP_001253990.1:p.Thr245=
NR_049782.2:n.1048G=
NR_049783.2:n.1021G=
NR_049784.2:n.997G=
NR_049785.2:n.930G=
NR_049786.2:n.879G=
NR_049787.2:n.730G=
NR_049788.2:n.660G=
NM_001267060.2:c.720G=	NP_001253989.1:p.Thr240=