Canonical Allele Identifier: CA346209682

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597944A>T (hg19) ; chr2:g.27375077A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375077A>T , CM000664.2:g.27375077A>T	GRCh38
NC_000002.11:g.27597944A>T , CM000664.1:g.27597944A>T	GRCh37
NC_000002.10:g.27451448A>T	NCBI36
NG_009305.1:g.381T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.698A>T MANE Select	ENSP00000233575.2:p.Glu233Val
ENST00000233575.6:c.698A>T	ENSP00000233575.2:p.Glu233Val
ENST00000427123.5:c.*508A>T	ENSP00000405399.1:n.*508A>T
ENST00000440760.5:c.*543A>T	ENSP00000399727.1:n.*543A>T
ENST00000453453.1:c.*225A>T	ENSP00000401922.1:n.*225A>T
ENST00000493711.1:n.415A>T
ENST00000494893.5:n.874A>T
ENST00000537606.5:c.623A>T	ENSP00000439208.1:p.Glu208Val
NM_001267059.1:c.662A>T	NP_001253988.1:p.Glu221Val
NM_001267060.1:c.623A>T	NP_001253989.1:p.Glu208Val
NM_001267061.1:c.638A>T	NP_001253990.1:p.Glu213Val
NM_014748.3:c.698A>T	NP_055563.1:p.Glu233Val
NR_049782.1:n.1071A>T
NR_049783.1:n.1044A>T
NR_049784.1:n.1020A>T
NR_049785.1:n.953A>T
NR_049786.1:n.902A>T
NR_049787.1:n.753A>T
NR_049788.1:n.683A>T
XM_011533203.1:c.56A>T	XP_011531505.1:p.Glu19Val
XM_011533203.2:c.56A>T	XP_011531505.1:p.Glu19Val
XM_017005405.2:c.56A>T	XP_016860894.1:p.Glu19Val
NM_014748.4:c.698A>T MANE Select	NP_055563.1:p.Glu233Val
NM_001267059.2:c.662A>T	NP_001253988.1:p.Glu221Val
NM_001267061.2:c.638A>T	NP_001253990.1:p.Glu213Val
NR_049782.2:n.951A>T
NR_049783.2:n.924A>T
NR_049784.2:n.900A>T
NR_049785.2:n.833A>T
NR_049786.2:n.782A>T
NR_049787.2:n.633A>T
NR_049788.2:n.563A>T
NM_001267060.2:c.623A>T	NP_001253989.1:p.Glu208Val