Canonical Allele Identifier: CA1240248008

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375093G= , CM000664.2:g.27375093G=	GRCh38
NC_000002.11:g.27597960G= , CM000664.1:g.27597960G=	GRCh37
NC_000002.10:g.27451464G=	NCBI36
NG_009305.1:g.365C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.714G= MANE Select	ENSP00000233575.2:p.Leu238=
ENST00000233575.6:c.714G=	ENSP00000233575.2:p.Leu238=
ENST00000427123.5:c.*524G=	ENSP00000405399.1:n.*524G=
ENST00000440760.5:c.*559G=	ENSP00000399727.1:n.*559G=
ENST00000453453.1:c.*241G=	ENSP00000401922.1:n.*241G=
ENST00000493711.1:n.431G=
ENST00000494893.5:n.890G=
ENST00000537606.5:c.639G=	ENSP00000439208.1:p.Leu213=
NM_001267059.1:c.678G=	NP_001253988.1:p.Leu226=
NM_001267060.1:c.639G=	NP_001253989.1:p.Leu213=
NM_001267061.1:c.654G=	NP_001253990.1:p.Leu218=
NM_014748.3:c.714G=	NP_055563.1:p.Leu238=
NR_049782.1:n.1087G=
NR_049783.1:n.1060G=
NR_049784.1:n.1036G=
NR_049785.1:n.969G=
NR_049786.1:n.918G=
NR_049787.1:n.769G=
NR_049788.1:n.699G=
XM_011533203.1:c.72G=	XP_011531505.1:p.Leu24=
XM_011533203.2:c.72G=	XP_011531505.1:p.Leu24=
XM_017005405.2:c.72G=	XP_016860894.1:p.Leu24=
NM_014748.4:c.714G= MANE Select	NP_055563.1:p.Leu238=
NM_001267059.2:c.678G=	NP_001253988.1:p.Leu226=
NM_001267061.2:c.654G=	NP_001253990.1:p.Leu218=
NR_049782.2:n.967G=
NR_049783.2:n.940G=
NR_049784.2:n.916G=
NR_049785.2:n.849G=
NR_049786.2:n.798G=
NR_049787.2:n.649G=
NR_049788.2:n.579G=
NM_001267060.2:c.639G=	NP_001253989.1:p.Leu213=