Canonical Allele Identifier: CA1240248659

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375510T= , CM000664.2:g.27375510T=	GRCh38
NC_000002.11:g.27598377T= , CM000664.1:g.27598377T=	GRCh37
NC_000002.10:g.27451881T=	NCBI36
NG_028219.1:g.10235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.779T= MANE Select	ENSP00000233575.2:p.Leu260=
ENST00000233575.6:c.779T=	ENSP00000233575.2:p.Leu260=
ENST00000427123.5:c.*589T=	ENSP00000405399.1:n.*589T=
ENST00000440760.5:c.*624T=	ENSP00000399727.1:n.*624T=
ENST00000453453.1:c.*306T=	ENSP00000401922.1:n.*306T=
ENST00000493711.1:n.496T=
ENST00000494893.5:n.955T=
ENST00000537606.5:c.704T=	ENSP00000439208.1:p.Leu235=
NM_001267059.1:c.743T=	NP_001253988.1:p.Leu248=
NM_001267060.1:c.704T=	NP_001253989.1:p.Leu235=
NM_001267061.1:c.719T=	NP_001253990.1:p.Leu240=
NM_014748.3:c.779T=	NP_055563.1:p.Leu260=
NR_049782.1:n.1152T=
NR_049783.1:n.1125T=
NR_049784.1:n.1101T=
NR_049785.1:n.1034T=
NR_049786.1:n.983T=
NR_049787.1:n.834T=
NR_049788.1:n.764T=
XM_011533203.1:c.137T=	XP_011531505.1:p.Leu46=
XM_011533203.2:c.137T=	XP_011531505.1:p.Leu46=
XM_017005405.2:c.137T=	XP_016860894.1:p.Leu46=
NM_014748.4:c.779T= MANE Select	NP_055563.1:p.Leu260=
NM_001267059.2:c.743T=	NP_001253988.1:p.Leu248=
NM_001267061.2:c.719T=	NP_001253990.1:p.Leu240=
NR_049782.2:n.1032T=
NR_049783.2:n.1005T=
NR_049784.2:n.981T=
NR_049785.2:n.914T=
NR_049786.2:n.863T=
NR_049787.2:n.714T=
NR_049788.2:n.644T=
NM_001267060.2:c.704T=	NP_001253989.1:p.Leu235=