Canonical Allele Identifier: CA425606810

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598381A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375514A>G , CM000664.2:g.27375514A>G	GRCh38
NC_000002.11:g.27598381A>G , CM000664.1:g.27598381A>G	GRCh37
NC_000002.10:g.27451885A>G	NCBI36
NG_028219.1:g.10231T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.783A>G MANE Select	ENSP00000233575.2:p.Arg261=
ENST00000233575.6:c.783A>G	ENSP00000233575.2:p.Arg261=
ENST00000427123.5:c.*593A>G	ENSP00000405399.1:n.*593A>G
ENST00000440760.5:c.*628A>G	ENSP00000399727.1:n.*628A>G
ENST00000453453.1:c.*310A>G	ENSP00000401922.1:n.*310A>G
ENST00000493711.1:n.500A>G
ENST00000494893.5:n.959A>G
ENST00000537606.5:c.708A>G	ENSP00000439208.1:p.Arg236=
NM_001267059.1:c.747A>G	NP_001253988.1:p.Arg249=
NM_001267060.1:c.708A>G	NP_001253989.1:p.Arg236=
NM_001267061.1:c.723A>G	NP_001253990.1:p.Arg241=
NM_014748.3:c.783A>G	NP_055563.1:p.Arg261=
NR_049782.1:n.1156A>G
NR_049783.1:n.1129A>G
NR_049784.1:n.1105A>G
NR_049785.1:n.1038A>G
NR_049786.1:n.987A>G
NR_049787.1:n.838A>G
NR_049788.1:n.768A>G
XM_011533203.1:c.141A>G	XP_011531505.1:p.Arg47=
XM_011533203.2:c.141A>G	XP_011531505.1:p.Arg47=
XM_017005405.2:c.141A>G	XP_016860894.1:p.Arg47=
NM_014748.4:c.783A>G MANE Select	NP_055563.1:p.Arg261=
NM_001267059.2:c.747A>G	NP_001253988.1:p.Arg249=
NM_001267061.2:c.723A>G	NP_001253990.1:p.Arg241=
NR_049782.2:n.1036A>G
NR_049783.2:n.1009A>G
NR_049784.2:n.985A>G
NR_049785.2:n.918A>G
NR_049786.2:n.867A>G
NR_049787.2:n.718A>G
NR_049788.2:n.648A>G
NM_001267060.2:c.708A>G	NP_001253989.1:p.Arg236=