Canonical Allele Identifier: CA1240248052

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375142T= , CM000664.2:g.27375142T=	GRCh38
NC_000002.11:g.27598009T= , CM000664.1:g.27598009T=	GRCh37
NC_000002.10:g.27451513T=	NCBI36
NG_009305.1:g.316A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.763T= MANE Select	ENSP00000233575.2:p.Ser255=
ENST00000233575.6:c.763T=	ENSP00000233575.2:p.Ser255=
ENST00000427123.5:c.*573T=	ENSP00000405399.1:n.*573T=
ENST00000440760.5:c.*608T=	ENSP00000399727.1:n.*608T=
ENST00000453453.1:c.*290T=	ENSP00000401922.1:n.*290T=
ENST00000493711.1:n.480T=
ENST00000494893.5:n.939T=
ENST00000537606.5:c.688T=	ENSP00000439208.1:p.Ser230=
NM_001267059.1:c.727T=	NP_001253988.1:p.Ser243=
NM_001267060.1:c.688T=	NP_001253989.1:p.Ser230=
NM_001267061.1:c.703T=	NP_001253990.1:p.Ser235=
NM_014748.3:c.763T=	NP_055563.1:p.Ser255=
NR_049782.1:n.1136T=
NR_049783.1:n.1109T=
NR_049784.1:n.1085T=
NR_049785.1:n.1018T=
NR_049786.1:n.967T=
NR_049787.1:n.818T=
NR_049788.1:n.748T=
XM_011533203.1:c.121T=	XP_011531505.1:p.Ser41=
XM_011533203.2:c.121T=	XP_011531505.1:p.Ser41=
XM_017005405.2:c.121T=	XP_016860894.1:p.Ser41=
NM_014748.4:c.763T= MANE Select	NP_055563.1:p.Ser255=
NM_001267059.2:c.727T=	NP_001253988.1:p.Ser243=
NM_001267061.2:c.703T=	NP_001253990.1:p.Ser235=
NR_049782.2:n.1016T=
NR_049783.2:n.989T=
NR_049784.2:n.965T=
NR_049785.2:n.898T=
NR_049786.2:n.847T=
NR_049787.2:n.698T=
NR_049788.2:n.628T=
NM_001267060.2:c.688T=	NP_001253989.1:p.Ser230=