Canonical Allele Identifier: CA1240247994

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375081T= , CM000664.2:g.27375081T=	GRCh38
NC_000002.11:g.27597948T= , CM000664.1:g.27597948T=	GRCh37
NC_000002.10:g.27451452T=	NCBI36
NG_009305.1:g.377A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.702T= MANE Select	ENSP00000233575.2:p.Arg234=
ENST00000233575.6:c.702T=	ENSP00000233575.2:p.Arg234=
ENST00000427123.5:c.*512T=	ENSP00000405399.1:n.*512T=
ENST00000440760.5:c.*547T=	ENSP00000399727.1:n.*547T=
ENST00000453453.1:c.*229T=	ENSP00000401922.1:n.*229T=
ENST00000493711.1:n.419T=
ENST00000494893.5:n.878T=
ENST00000537606.5:c.627T=	ENSP00000439208.1:p.Arg209=
NM_001267059.1:c.666T=	NP_001253988.1:p.Arg222=
NM_001267060.1:c.627T=	NP_001253989.1:p.Arg209=
NM_001267061.1:c.642T=	NP_001253990.1:p.Arg214=
NM_014748.3:c.702T=	NP_055563.1:p.Arg234=
NR_049782.1:n.1075T=
NR_049783.1:n.1048T=
NR_049784.1:n.1024T=
NR_049785.1:n.957T=
NR_049786.1:n.906T=
NR_049787.1:n.757T=
NR_049788.1:n.687T=
XM_011533203.1:c.60T=	XP_011531505.1:p.Arg20=
XM_011533203.2:c.60T=	XP_011531505.1:p.Arg20=
XM_017005405.2:c.60T=	XP_016860894.1:p.Arg20=
NM_014748.4:c.702T= MANE Select	NP_055563.1:p.Arg234=
NM_001267059.2:c.666T=	NP_001253988.1:p.Arg222=
NM_001267061.2:c.642T=	NP_001253990.1:p.Arg214=
NR_049782.2:n.955T=
NR_049783.2:n.928T=
NR_049784.2:n.904T=
NR_049785.2:n.837T=
NR_049786.2:n.786T=
NR_049787.2:n.637T=
NR_049788.2:n.567T=
NM_001267060.2:c.627T=	NP_001253989.1:p.Arg209=