Canonical Allele Identifier: CA1240248000

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375087G= , CM000664.2:g.27375087G=	GRCh38
NC_000002.11:g.27597954G= , CM000664.1:g.27597954G=	GRCh37
NC_000002.10:g.27451458G=	NCBI36
NG_009305.1:g.371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.708G= MANE Select	ENSP00000233575.2:p.Trp236=
ENST00000233575.6:c.708G=	ENSP00000233575.2:p.Trp236=
ENST00000427123.5:c.*518G=	ENSP00000405399.1:n.*518G=
ENST00000440760.5:c.*553G=	ENSP00000399727.1:n.*553G=
ENST00000453453.1:c.*235G=	ENSP00000401922.1:n.*235G=
ENST00000493711.1:n.425G=
ENST00000494893.5:n.884G=
ENST00000537606.5:c.633G=	ENSP00000439208.1:p.Trp211=
NM_001267059.1:c.672G=	NP_001253988.1:p.Trp224=
NM_001267060.1:c.633G=	NP_001253989.1:p.Trp211=
NM_001267061.1:c.648G=	NP_001253990.1:p.Trp216=
NM_014748.3:c.708G=	NP_055563.1:p.Trp236=
NR_049782.1:n.1081G=
NR_049783.1:n.1054G=
NR_049784.1:n.1030G=
NR_049785.1:n.963G=
NR_049786.1:n.912G=
NR_049787.1:n.763G=
NR_049788.1:n.693G=
XM_011533203.1:c.66G=	XP_011531505.1:p.Trp22=
XM_011533203.2:c.66G=	XP_011531505.1:p.Trp22=
XM_017005405.2:c.66G=	XP_016860894.1:p.Trp22=
NM_014748.4:c.708G= MANE Select	NP_055563.1:p.Trp236=
NM_001267059.2:c.672G=	NP_001253988.1:p.Trp224=
NM_001267061.2:c.648G=	NP_001253990.1:p.Trp216=
NR_049782.2:n.961G=
NR_049783.2:n.934G=
NR_049784.2:n.910G=
NR_049785.2:n.843G=
NR_049786.2:n.792G=
NR_049787.2:n.643G=
NR_049788.2:n.573G=
NM_001267060.2:c.633G=	NP_001253989.1:p.Trp211=