Canonical Allele Identifier: CA1240248703

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375525C= , CM000664.2:g.27375525C=	GRCh38
NC_000002.11:g.27598392C= , CM000664.1:g.27598392C=	GRCh37
NC_000002.10:g.27451896C=	NCBI36
NG_028219.1:g.10220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.794C= MANE Select	ENSP00000233575.2:p.Thr265=
ENST00000233575.6:c.794C=	ENSP00000233575.2:p.Thr265=
ENST00000427123.5:c.*604C=	ENSP00000405399.1:n.*604C=
ENST00000440760.5:c.*639C=	ENSP00000399727.1:n.*639C=
ENST00000453453.1:c.*321C=	ENSP00000401922.1:n.*321C=
ENST00000493711.1:n.511C=
ENST00000537606.5:c.719C=	ENSP00000439208.1:p.Thr240=
NM_001267059.1:c.758C=	NP_001253988.1:p.Thr253=
NM_001267060.1:c.719C=	NP_001253989.1:p.Thr240=
NM_001267061.1:c.734C=	NP_001253990.1:p.Thr245=
NM_014748.3:c.794C=	NP_055563.1:p.Thr265=
NR_049782.1:n.1167C=
NR_049783.1:n.1140C=
NR_049784.1:n.1116C=
NR_049785.1:n.1049C=
NR_049786.1:n.998C=
NR_049787.1:n.849C=
NR_049788.1:n.779C=
XM_011533203.1:c.152C=	XP_011531505.1:p.Thr51=
XM_011533203.2:c.152C=	XP_011531505.1:p.Thr51=
XM_017005405.2:c.152C=	XP_016860894.1:p.Thr51=
NM_014748.4:c.794C= MANE Select	NP_055563.1:p.Thr265=
NM_001267059.2:c.758C=	NP_001253988.1:p.Thr253=
NM_001267061.2:c.734C=	NP_001253990.1:p.Thr245=
NR_049782.2:n.1047C=
NR_049783.2:n.1020C=
NR_049784.2:n.996C=
NR_049785.2:n.929C=
NR_049786.2:n.878C=
NR_049787.2:n.729C=
NR_049788.2:n.659C=
NM_001267060.2:c.719C=	NP_001253989.1:p.Thr240=