Canonical Allele Identifier: CA1240248035

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375118C= , CM000664.2:g.27375118C=	GRCh38
NC_000002.11:g.27597985C= , CM000664.1:g.27597985C=	GRCh37
NC_000002.10:g.27451489C=	NCBI36
NG_009305.1:g.340G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.739C= MANE Select	ENSP00000233575.2:p.Leu247=
ENST00000233575.6:c.739C=	ENSP00000233575.2:p.Leu247=
ENST00000427123.5:c.*549C=	ENSP00000405399.1:n.*549C=
ENST00000440760.5:c.*584C=	ENSP00000399727.1:n.*584C=
ENST00000453453.1:c.*266C=	ENSP00000401922.1:n.*266C=
ENST00000493711.1:n.456C=
ENST00000494893.5:n.915C=
ENST00000537606.5:c.664C=	ENSP00000439208.1:p.Leu222=
NM_001267059.1:c.703C=	NP_001253988.1:p.Leu235=
NM_001267060.1:c.664C=	NP_001253989.1:p.Leu222=
NM_001267061.1:c.679C=	NP_001253990.1:p.Leu227=
NM_014748.3:c.739C=	NP_055563.1:p.Leu247=
NR_049782.1:n.1112C=
NR_049783.1:n.1085C=
NR_049784.1:n.1061C=
NR_049785.1:n.994C=
NR_049786.1:n.943C=
NR_049787.1:n.794C=
NR_049788.1:n.724C=
XM_011533203.1:c.97C=	XP_011531505.1:p.Leu33=
XM_011533203.2:c.97C=	XP_011531505.1:p.Leu33=
XM_017005405.2:c.97C=	XP_016860894.1:p.Leu33=
NM_014748.4:c.739C= MANE Select	NP_055563.1:p.Leu247=
NM_001267059.2:c.703C=	NP_001253988.1:p.Leu235=
NM_001267061.2:c.679C=	NP_001253990.1:p.Leu227=
NR_049782.2:n.992C=
NR_049783.2:n.965C=
NR_049784.2:n.941C=
NR_049785.2:n.874C=
NR_049786.2:n.823C=
NR_049787.2:n.674C=
NR_049788.2:n.604C=
NM_001267060.2:c.664C=	NP_001253989.1:p.Leu222=