Canonical Allele Identifier: CA1240248042

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375122A= , CM000664.2:g.27375122A=	GRCh38
NC_000002.11:g.27597989A= , CM000664.1:g.27597989A=	GRCh37
NC_000002.10:g.27451493A=	NCBI36
NG_009305.1:g.336T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.743A= MANE Select	ENSP00000233575.2:p.Lys248=
ENST00000233575.6:c.743A=	ENSP00000233575.2:p.Lys248=
ENST00000427123.5:c.*553A=	ENSP00000405399.1:n.*553A=
ENST00000440760.5:c.*588A=	ENSP00000399727.1:n.*588A=
ENST00000453453.1:c.*270A=	ENSP00000401922.1:n.*270A=
ENST00000493711.1:n.460A=
ENST00000494893.5:n.919A=
ENST00000537606.5:c.668A=	ENSP00000439208.1:p.Lys223=
NM_001267059.1:c.707A=	NP_001253988.1:p.Lys236=
NM_001267060.1:c.668A=	NP_001253989.1:p.Lys223=
NM_001267061.1:c.683A=	NP_001253990.1:p.Lys228=
NM_014748.3:c.743A=	NP_055563.1:p.Lys248=
NR_049782.1:n.1116A=
NR_049783.1:n.1089A=
NR_049784.1:n.1065A=
NR_049785.1:n.998A=
NR_049786.1:n.947A=
NR_049787.1:n.798A=
NR_049788.1:n.728A=
XM_011533203.1:c.101A=	XP_011531505.1:p.Lys34=
XM_011533203.2:c.101A=	XP_011531505.1:p.Lys34=
XM_017005405.2:c.101A=	XP_016860894.1:p.Lys34=
NM_014748.4:c.743A= MANE Select	NP_055563.1:p.Lys248=
NM_001267059.2:c.707A=	NP_001253988.1:p.Lys236=
NM_001267061.2:c.683A=	NP_001253990.1:p.Lys228=
NR_049782.2:n.996A=
NR_049783.2:n.969A=
NR_049784.2:n.945A=
NR_049785.2:n.878A=
NR_049786.2:n.827A=
NR_049787.2:n.678A=
NR_049788.2:n.608A=
NM_001267060.2:c.668A=	NP_001253989.1:p.Lys223=