Canonical Allele Identifier: CA1240248026

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375111C= , CM000664.2:g.27375111C=	GRCh38
NC_000002.11:g.27597978C= , CM000664.1:g.27597978C=	GRCh37
NC_000002.10:g.27451482C=	NCBI36
NG_009305.1:g.347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.732C= MANE Select	ENSP00000233575.2:p.His244=
ENST00000233575.6:c.732C=	ENSP00000233575.2:p.His244=
ENST00000427123.5:c.*542C=	ENSP00000405399.1:n.*542C=
ENST00000440760.5:c.*577C=	ENSP00000399727.1:n.*577C=
ENST00000453453.1:c.*259C=	ENSP00000401922.1:n.*259C=
ENST00000493711.1:n.449C=
ENST00000494893.5:n.908C=
ENST00000537606.5:c.657C=	ENSP00000439208.1:p.His219=
NM_001267059.1:c.696C=	NP_001253988.1:p.His232=
NM_001267060.1:c.657C=	NP_001253989.1:p.His219=
NM_001267061.1:c.672C=	NP_001253990.1:p.His224=
NM_014748.3:c.732C=	NP_055563.1:p.His244=
NR_049782.1:n.1105C=
NR_049783.1:n.1078C=
NR_049784.1:n.1054C=
NR_049785.1:n.987C=
NR_049786.1:n.936C=
NR_049787.1:n.787C=
NR_049788.1:n.717C=
XM_011533203.1:c.90C=	XP_011531505.1:p.His30=
XM_011533203.2:c.90C=	XP_011531505.1:p.His30=
XM_017005405.2:c.90C=	XP_016860894.1:p.His30=
NM_014748.4:c.732C= MANE Select	NP_055563.1:p.His244=
NM_001267059.2:c.696C=	NP_001253988.1:p.His232=
NM_001267061.2:c.672C=	NP_001253990.1:p.His224=
NR_049782.2:n.985C=
NR_049783.2:n.958C=
NR_049784.2:n.934C=
NR_049785.2:n.867C=
NR_049786.2:n.816C=
NR_049787.2:n.667C=
NR_049788.2:n.597C=
NM_001267060.2:c.657C=	NP_001253989.1:p.His219=