Canonical Allele Identifier: CA1240248019

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375103G= , CM000664.2:g.27375103G=	GRCh38
NC_000002.11:g.27597970G= , CM000664.1:g.27597970G=	GRCh37
NC_000002.10:g.27451474G=	NCBI36
NG_009305.1:g.355C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.724G= MANE Select	ENSP00000233575.2:p.Glu242=
ENST00000233575.6:c.724G=	ENSP00000233575.2:p.Glu242=
ENST00000427123.5:c.*534G=	ENSP00000405399.1:n.*534G=
ENST00000440760.5:c.*569G=	ENSP00000399727.1:n.*569G=
ENST00000453453.1:c.*251G=	ENSP00000401922.1:n.*251G=
ENST00000493711.1:n.441G=
ENST00000494893.5:n.900G=
ENST00000537606.5:c.649G=	ENSP00000439208.1:p.Glu217=
NM_001267059.1:c.688G=	NP_001253988.1:p.Glu230=
NM_001267060.1:c.649G=	NP_001253989.1:p.Glu217=
NM_001267061.1:c.664G=	NP_001253990.1:p.Glu222=
NM_014748.3:c.724G=	NP_055563.1:p.Glu242=
NR_049782.1:n.1097G=
NR_049783.1:n.1070G=
NR_049784.1:n.1046G=
NR_049785.1:n.979G=
NR_049786.1:n.928G=
NR_049787.1:n.779G=
NR_049788.1:n.709G=
XM_011533203.1:c.82G=	XP_011531505.1:p.Glu28=
XM_011533203.2:c.82G=	XP_011531505.1:p.Glu28=
XM_017005405.2:c.82G=	XP_016860894.1:p.Glu28=
NM_014748.4:c.724G= MANE Select	NP_055563.1:p.Glu242=
NM_001267059.2:c.688G=	NP_001253988.1:p.Glu230=
NM_001267061.2:c.664G=	NP_001253990.1:p.Glu222=
NR_049782.2:n.977G=
NR_049783.2:n.950G=
NR_049784.2:n.926G=
NR_049785.2:n.859G=
NR_049786.2:n.808G=
NR_049787.2:n.659G=
NR_049788.2:n.589G=
NM_001267060.2:c.649G=	NP_001253989.1:p.Glu217=