Canonical Allele Identifier: CA1240248054

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375146A= , CM000664.2:g.27375146A=	GRCh38
NC_000002.11:g.27598013A= , CM000664.1:g.27598013A=	GRCh37
NC_000002.10:g.27451517A=	NCBI36
NG_009305.1:g.312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.767A= MANE Select	ENSP00000233575.2:p.Lys256=
ENST00000233575.6:c.767A=	ENSP00000233575.2:p.Lys256=
ENST00000427123.5:c.*577A=	ENSP00000405399.1:n.*577A=
ENST00000440760.5:c.*612A=	ENSP00000399727.1:n.*612A=
ENST00000453453.1:c.*294A=	ENSP00000401922.1:n.*294A=
ENST00000493711.1:n.484A=
ENST00000494893.5:n.943A=
ENST00000537606.5:c.692A=	ENSP00000439208.1:p.Lys231=
NM_001267059.1:c.731A=	NP_001253988.1:p.Lys244=
NM_001267060.1:c.692A=	NP_001253989.1:p.Lys231=
NM_001267061.1:c.707A=	NP_001253990.1:p.Lys236=
NM_014748.3:c.767A=	NP_055563.1:p.Lys256=
NR_049782.1:n.1140A=
NR_049783.1:n.1113A=
NR_049784.1:n.1089A=
NR_049785.1:n.1022A=
NR_049786.1:n.971A=
NR_049787.1:n.822A=
NR_049788.1:n.752A=
XM_011533203.1:c.125A=	XP_011531505.1:p.Lys42=
XM_011533203.2:c.125A=	XP_011531505.1:p.Lys42=
XM_017005405.2:c.125A=	XP_016860894.1:p.Lys42=
NM_014748.4:c.767A= MANE Select	NP_055563.1:p.Lys256=
NM_001267059.2:c.731A=	NP_001253988.1:p.Lys244=
NM_001267061.2:c.707A=	NP_001253990.1:p.Lys236=
NR_049782.2:n.1020A=
NR_049783.2:n.993A=
NR_049784.2:n.969A=
NR_049785.2:n.902A=
NR_049786.2:n.851A=
NR_049787.2:n.702A=
NR_049788.2:n.632A=
NM_001267060.2:c.692A=	NP_001253989.1:p.Lys231=