Canonical Allele Identifier: CA1240247989

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375079C= , CM000664.2:g.27375079C=	GRCh38
NC_000002.11:g.27597946C= , CM000664.1:g.27597946C=	GRCh37
NC_000002.10:g.27451450C=	NCBI36
NG_009305.1:g.379G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.700C= MANE Select	ENSP00000233575.2:p.Arg234=
ENST00000233575.6:c.700C=	ENSP00000233575.2:p.Arg234=
ENST00000427123.5:c.*510C=	ENSP00000405399.1:n.*510C=
ENST00000440760.5:c.*545C=	ENSP00000399727.1:n.*545C=
ENST00000453453.1:c.*227C=	ENSP00000401922.1:n.*227C=
ENST00000493711.1:n.417C=
ENST00000494893.5:n.876C=
ENST00000537606.5:c.625C=	ENSP00000439208.1:p.Arg209=
NM_001267059.1:c.664C=	NP_001253988.1:p.Arg222=
NM_001267060.1:c.625C=	NP_001253989.1:p.Arg209=
NM_001267061.1:c.640C=	NP_001253990.1:p.Arg214=
NM_014748.3:c.700C=	NP_055563.1:p.Arg234=
NR_049782.1:n.1073C=
NR_049783.1:n.1046C=
NR_049784.1:n.1022C=
NR_049785.1:n.955C=
NR_049786.1:n.904C=
NR_049787.1:n.755C=
NR_049788.1:n.685C=
XM_011533203.1:c.58C=	XP_011531505.1:p.Arg20=
XM_011533203.2:c.58C=	XP_011531505.1:p.Arg20=
XM_017005405.2:c.58C=	XP_016860894.1:p.Arg20=
NM_014748.4:c.700C= MANE Select	NP_055563.1:p.Arg234=
NM_001267059.2:c.664C=	NP_001253988.1:p.Arg222=
NM_001267061.2:c.640C=	NP_001253990.1:p.Arg214=
NR_049782.2:n.953C=
NR_049783.2:n.926C=
NR_049784.2:n.902C=
NR_049785.2:n.835C=
NR_049786.2:n.784C=
NR_049787.2:n.635C=
NR_049788.2:n.565C=
NM_001267060.2:c.625C=	NP_001253989.1:p.Arg209=