Canonical Allele Identifier: CA1240248037

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375120C= , CM000664.2:g.27375120C=	GRCh38
NC_000002.11:g.27597987C= , CM000664.1:g.27597987C=	GRCh37
NC_000002.10:g.27451491C=	NCBI36
NG_009305.1:g.338G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.741C= MANE Select	ENSP00000233575.2:p.Leu247=
ENST00000233575.6:c.741C=	ENSP00000233575.2:p.Leu247=
ENST00000427123.5:c.*551C=	ENSP00000405399.1:n.*551C=
ENST00000440760.5:c.*586C=	ENSP00000399727.1:n.*586C=
ENST00000453453.1:c.*268C=	ENSP00000401922.1:n.*268C=
ENST00000493711.1:n.458C=
ENST00000494893.5:n.917C=
ENST00000537606.5:c.666C=	ENSP00000439208.1:p.Leu222=
NM_001267059.1:c.705C=	NP_001253988.1:p.Leu235=
NM_001267060.1:c.666C=	NP_001253989.1:p.Leu222=
NM_001267061.1:c.681C=	NP_001253990.1:p.Leu227=
NM_014748.3:c.741C=	NP_055563.1:p.Leu247=
NR_049782.1:n.1114C=
NR_049783.1:n.1087C=
NR_049784.1:n.1063C=
NR_049785.1:n.996C=
NR_049786.1:n.945C=
NR_049787.1:n.796C=
NR_049788.1:n.726C=
XM_011533203.1:c.99C=	XP_011531505.1:p.Leu33=
XM_011533203.2:c.99C=	XP_011531505.1:p.Leu33=
XM_017005405.2:c.99C=	XP_016860894.1:p.Leu33=
NM_014748.4:c.741C= MANE Select	NP_055563.1:p.Leu247=
NM_001267059.2:c.705C=	NP_001253988.1:p.Leu235=
NM_001267061.2:c.681C=	NP_001253990.1:p.Leu227=
NR_049782.2:n.994C=
NR_049783.2:n.967C=
NR_049784.2:n.943C=
NR_049785.2:n.876C=
NR_049786.2:n.825C=
NR_049787.2:n.676C=
NR_049788.2:n.606C=
NM_001267060.2:c.666C=	NP_001253989.1:p.Leu222=