Canonical Allele Identifier: CA1240248047

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375138A= , CM000664.2:g.27375138A=	GRCh38
NC_000002.11:g.27598005A= , CM000664.1:g.27598005A=	GRCh37
NC_000002.10:g.27451509A=	NCBI36
NG_009305.1:g.320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.759A= MANE Select	ENSP00000233575.2:p.Lys253=
ENST00000233575.6:c.759A=	ENSP00000233575.2:p.Lys253=
ENST00000427123.5:c.*569A=	ENSP00000405399.1:n.*569A=
ENST00000440760.5:c.*604A=	ENSP00000399727.1:n.*604A=
ENST00000453453.1:c.*286A=	ENSP00000401922.1:n.*286A=
ENST00000493711.1:n.476A=
ENST00000494893.5:n.935A=
ENST00000537606.5:c.684A=	ENSP00000439208.1:p.Lys228=
NM_001267059.1:c.723A=	NP_001253988.1:p.Lys241=
NM_001267060.1:c.684A=	NP_001253989.1:p.Lys228=
NM_001267061.1:c.699A=	NP_001253990.1:p.Lys233=
NM_014748.3:c.759A=	NP_055563.1:p.Lys253=
NR_049782.1:n.1132A=
NR_049783.1:n.1105A=
NR_049784.1:n.1081A=
NR_049785.1:n.1014A=
NR_049786.1:n.963A=
NR_049787.1:n.814A=
NR_049788.1:n.744A=
XM_011533203.1:c.117A=	XP_011531505.1:p.Lys39=
XM_011533203.2:c.117A=	XP_011531505.1:p.Lys39=
XM_017005405.2:c.117A=	XP_016860894.1:p.Lys39=
NM_014748.4:c.759A= MANE Select	NP_055563.1:p.Lys253=
NM_001267059.2:c.723A=	NP_001253988.1:p.Lys241=
NM_001267061.2:c.699A=	NP_001253990.1:p.Lys233=
NR_049782.2:n.1012A=
NR_049783.2:n.985A=
NR_049784.2:n.961A=
NR_049785.2:n.894A=
NR_049786.2:n.843A=
NR_049787.2:n.694A=
NR_049788.2:n.624A=
NM_001267060.2:c.684A=	NP_001253989.1:p.Lys228=