Canonical Allele Identifier: CA1240247996

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375086G= , CM000664.2:g.27375086G=	GRCh38
NC_000002.11:g.27597953G= , CM000664.1:g.27597953G=	GRCh37
NC_000002.10:g.27451457G=	NCBI36
NG_009305.1:g.372C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.707G= MANE Select	ENSP00000233575.2:p.Trp236=
ENST00000233575.6:c.707G=	ENSP00000233575.2:p.Trp236=
ENST00000427123.5:c.*517G=	ENSP00000405399.1:n.*517G=
ENST00000440760.5:c.*552G=	ENSP00000399727.1:n.*552G=
ENST00000453453.1:c.*234G=	ENSP00000401922.1:n.*234G=
ENST00000493711.1:n.424G=
ENST00000494893.5:n.883G=
ENST00000537606.5:c.632G=	ENSP00000439208.1:p.Trp211=
NM_001267059.1:c.671G=	NP_001253988.1:p.Trp224=
NM_001267060.1:c.632G=	NP_001253989.1:p.Trp211=
NM_001267061.1:c.647G=	NP_001253990.1:p.Trp216=
NM_014748.3:c.707G=	NP_055563.1:p.Trp236=
NR_049782.1:n.1080G=
NR_049783.1:n.1053G=
NR_049784.1:n.1029G=
NR_049785.1:n.962G=
NR_049786.1:n.911G=
NR_049787.1:n.762G=
NR_049788.1:n.692G=
XM_011533203.1:c.65G=	XP_011531505.1:p.Trp22=
XM_011533203.2:c.65G=	XP_011531505.1:p.Trp22=
XM_017005405.2:c.65G=	XP_016860894.1:p.Trp22=
NM_014748.4:c.707G= MANE Select	NP_055563.1:p.Trp236=
NM_001267059.2:c.671G=	NP_001253988.1:p.Trp224=
NM_001267061.2:c.647G=	NP_001253990.1:p.Trp216=
NR_049782.2:n.960G=
NR_049783.2:n.933G=
NR_049784.2:n.909G=
NR_049785.2:n.842G=
NR_049786.2:n.791G=
NR_049787.2:n.642G=
NR_049788.2:n.572G=
NM_001267060.2:c.632G=	NP_001253989.1:p.Trp211=