Canonical Allele Identifier: CA1240248024

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375106C= , CM000664.2:g.27375106C=	GRCh38
NC_000002.11:g.27597973C= , CM000664.1:g.27597973C=	GRCh37
NC_000002.10:g.27451477C=	NCBI36
NG_009305.1:g.352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.727C= MANE Select	ENSP00000233575.2:p.Gln243=
ENST00000233575.6:c.727C=	ENSP00000233575.2:p.Gln243=
ENST00000427123.5:c.*537C=	ENSP00000405399.1:n.*537C=
ENST00000440760.5:c.*572C=	ENSP00000399727.1:n.*572C=
ENST00000453453.1:c.*254C=	ENSP00000401922.1:n.*254C=
ENST00000493711.1:n.444C=
ENST00000494893.5:n.903C=
ENST00000537606.5:c.652C=	ENSP00000439208.1:p.Gln218=
NM_001267059.1:c.691C=	NP_001253988.1:p.Gln231=
NM_001267060.1:c.652C=	NP_001253989.1:p.Gln218=
NM_001267061.1:c.667C=	NP_001253990.1:p.Gln223=
NM_014748.3:c.727C=	NP_055563.1:p.Gln243=
NR_049782.1:n.1100C=
NR_049783.1:n.1073C=
NR_049784.1:n.1049C=
NR_049785.1:n.982C=
NR_049786.1:n.931C=
NR_049787.1:n.782C=
NR_049788.1:n.712C=
XM_011533203.1:c.85C=	XP_011531505.1:p.Gln29=
XM_011533203.2:c.85C=	XP_011531505.1:p.Gln29=
XM_017005405.2:c.85C=	XP_016860894.1:p.Gln29=
NM_014748.4:c.727C= MANE Select	NP_055563.1:p.Gln243=
NM_001267059.2:c.691C=	NP_001253988.1:p.Gln231=
NM_001267061.2:c.667C=	NP_001253990.1:p.Gln223=
NR_049782.2:n.980C=
NR_049783.2:n.953C=
NR_049784.2:n.929C=
NR_049785.2:n.862C=
NR_049786.2:n.811C=
NR_049787.2:n.662C=
NR_049788.2:n.592C=
NM_001267060.2:c.652C=	NP_001253989.1:p.Gln218=