Canonical Allele Identifier: CA1240247992

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375080G= , CM000664.2:g.27375080G=	GRCh38
NC_000002.11:g.27597947G= , CM000664.1:g.27597947G=	GRCh37
NC_000002.10:g.27451451G=	NCBI36
NG_009305.1:g.378C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.701G= MANE Select	ENSP00000233575.2:p.Arg234=
ENST00000233575.6:c.701G=	ENSP00000233575.2:p.Arg234=
ENST00000427123.5:c.*511G=	ENSP00000405399.1:n.*511G=
ENST00000440760.5:c.*546G=	ENSP00000399727.1:n.*546G=
ENST00000453453.1:c.*228G=	ENSP00000401922.1:n.*228G=
ENST00000493711.1:n.418G=
ENST00000494893.5:n.877G=
ENST00000537606.5:c.626G=	ENSP00000439208.1:p.Arg209=
NM_001267059.1:c.665G=	NP_001253988.1:p.Arg222=
NM_001267060.1:c.626G=	NP_001253989.1:p.Arg209=
NM_001267061.1:c.641G=	NP_001253990.1:p.Arg214=
NM_014748.3:c.701G=	NP_055563.1:p.Arg234=
NR_049782.1:n.1074G=
NR_049783.1:n.1047G=
NR_049784.1:n.1023G=
NR_049785.1:n.956G=
NR_049786.1:n.905G=
NR_049787.1:n.756G=
NR_049788.1:n.686G=
XM_011533203.1:c.59G=	XP_011531505.1:p.Arg20=
XM_011533203.2:c.59G=	XP_011531505.1:p.Arg20=
XM_017005405.2:c.59G=	XP_016860894.1:p.Arg20=
NM_014748.4:c.701G= MANE Select	NP_055563.1:p.Arg234=
NM_001267059.2:c.665G=	NP_001253988.1:p.Arg222=
NM_001267061.2:c.641G=	NP_001253990.1:p.Arg214=
NR_049782.2:n.954G=
NR_049783.2:n.927G=
NR_049784.2:n.903G=
NR_049785.2:n.836G=
NR_049786.2:n.785G=
NR_049787.2:n.636G=
NR_049788.2:n.566G=
NM_001267060.2:c.626G=	NP_001253989.1:p.Arg209=