Canonical Allele Identifier: CA1240249435

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375062C= , CM000664.2:g.27375062C=	GRCh38
NC_000002.11:g.27597929C= , CM000664.1:g.27597929C=	GRCh37
NC_000002.10:g.27451433C=	NCBI36
NG_009305.1:g.396G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.683C= MANE Select	ENSP00000233575.2:p.Thr228=
ENST00000233575.6:c.683C=	ENSP00000233575.2:p.Thr228=
ENST00000427123.5:c.*493C=	ENSP00000405399.1:n.*493C=
ENST00000440760.5:c.*528C=	ENSP00000399727.1:n.*528C=
ENST00000453453.1:c.*210C=	ENSP00000401922.1:n.*210C=
ENST00000493711.1:n.400C=
ENST00000494893.5:n.859C=
ENST00000537606.5:c.608C=	ENSP00000439208.1:p.Thr203=
NM_001267059.1:c.647C=	NP_001253988.1:p.Thr216=
NM_001267060.1:c.608C=	NP_001253989.1:p.Thr203=
NM_001267061.1:c.623C=	NP_001253990.1:p.Thr208=
NM_014748.3:c.683C=	NP_055563.1:p.Thr228=
NR_049782.1:n.1056C=
NR_049783.1:n.1029C=
NR_049784.1:n.1005C=
NR_049785.1:n.938C=
NR_049786.1:n.887C=
NR_049787.1:n.738C=
NR_049788.1:n.668C=
XM_011533203.1:c.41C=	XP_011531505.1:p.Thr14=
XM_011533203.2:c.41C=	XP_011531505.1:p.Thr14=
XM_017005405.2:c.41C=	XP_016860894.1:p.Thr14=
NM_014748.4:c.683C= MANE Select	NP_055563.1:p.Thr228=
NM_001267059.2:c.647C=	NP_001253988.1:p.Thr216=
NM_001267061.2:c.623C=	NP_001253990.1:p.Thr208=
NR_049782.2:n.936C=
NR_049783.2:n.909C=
NR_049784.2:n.885C=
NR_049785.2:n.818C=
NR_049786.2:n.767C=
NR_049787.2:n.618C=
NR_049788.2:n.548C=
NM_001267060.2:c.608C=	NP_001253989.1:p.Thr203=