Canonical Allele Identifier: CA1240247987

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375074T= , CM000664.2:g.27375074T=	GRCh38
NC_000002.11:g.27597941T= , CM000664.1:g.27597941T=	GRCh37
NC_000002.10:g.27451445T=	NCBI36
NG_009305.1:g.384A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.695T= MANE Select	ENSP00000233575.2:p.Ile232=
ENST00000233575.6:c.695T=	ENSP00000233575.2:p.Ile232=
ENST00000427123.5:c.*505T=	ENSP00000405399.1:n.*505T=
ENST00000440760.5:c.*540T=	ENSP00000399727.1:n.*540T=
ENST00000453453.1:c.*222T=	ENSP00000401922.1:n.*222T=
ENST00000493711.1:n.412T=
ENST00000494893.5:n.871T=
ENST00000537606.5:c.620T=	ENSP00000439208.1:p.Ile207=
NM_001267059.1:c.659T=	NP_001253988.1:p.Ile220=
NM_001267060.1:c.620T=	NP_001253989.1:p.Ile207=
NM_001267061.1:c.635T=	NP_001253990.1:p.Ile212=
NM_014748.3:c.695T=	NP_055563.1:p.Ile232=
NR_049782.1:n.1068T=
NR_049783.1:n.1041T=
NR_049784.1:n.1017T=
NR_049785.1:n.950T=
NR_049786.1:n.899T=
NR_049787.1:n.750T=
NR_049788.1:n.680T=
XM_011533203.1:c.53T=	XP_011531505.1:p.Ile18=
XM_011533203.2:c.53T=	XP_011531505.1:p.Ile18=
XM_017005405.2:c.53T=	XP_016860894.1:p.Ile18=
NM_014748.4:c.695T= MANE Select	NP_055563.1:p.Ile232=
NM_001267059.2:c.659T=	NP_001253988.1:p.Ile220=
NM_001267061.2:c.635T=	NP_001253990.1:p.Ile212=
NR_049782.2:n.948T=
NR_049783.2:n.921T=
NR_049784.2:n.897T=
NR_049785.2:n.830T=
NR_049786.2:n.779T=
NR_049787.2:n.630T=
NR_049788.2:n.560T=
NM_001267060.2:c.620T=	NP_001253989.1:p.Ile207=