Canonical Allele Identifier: CA1240249450

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375068C= , CM000664.2:g.27375068C=	GRCh38
NC_000002.11:g.27597935C= , CM000664.1:g.27597935C=	GRCh37
NC_000002.10:g.27451439C=	NCBI36
NG_009305.1:g.390G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.689C= MANE Select	ENSP00000233575.2:p.Ser230=
ENST00000233575.6:c.689C=	ENSP00000233575.2:p.Ser230=
ENST00000427123.5:c.*499C=	ENSP00000405399.1:n.*499C=
ENST00000440760.5:c.*534C=	ENSP00000399727.1:n.*534C=
ENST00000453453.1:c.*216C=	ENSP00000401922.1:n.*216C=
ENST00000493711.1:n.406C=
ENST00000494893.5:n.865C=
ENST00000537606.5:c.614C=	ENSP00000439208.1:p.Ser205=
NM_001267059.1:c.653C=	NP_001253988.1:p.Ser218=
NM_001267060.1:c.614C=	NP_001253989.1:p.Ser205=
NM_001267061.1:c.629C=	NP_001253990.1:p.Ser210=
NM_014748.3:c.689C=	NP_055563.1:p.Ser230=
NR_049782.1:n.1062C=
NR_049783.1:n.1035C=
NR_049784.1:n.1011C=
NR_049785.1:n.944C=
NR_049786.1:n.893C=
NR_049787.1:n.744C=
NR_049788.1:n.674C=
XM_011533203.1:c.47C=	XP_011531505.1:p.Ser16=
XM_011533203.2:c.47C=	XP_011531505.1:p.Ser16=
XM_017005405.2:c.47C=	XP_016860894.1:p.Ser16=
NM_014748.4:c.689C= MANE Select	NP_055563.1:p.Ser230=
NM_001267059.2:c.653C=	NP_001253988.1:p.Ser218=
NM_001267061.2:c.629C=	NP_001253990.1:p.Ser210=
NR_049782.2:n.942C=
NR_049783.2:n.915C=
NR_049784.2:n.891C=
NR_049785.2:n.824C=
NR_049786.2:n.773C=
NR_049787.2:n.624C=
NR_049788.2:n.554C=
NM_001267060.2:c.614C=	NP_001253989.1:p.Ser205=