Canonical Allele Identifier: CA425415736

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597945G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375078G>A , CM000664.2:g.27375078G>A	GRCh38
NC_000002.11:g.27597945G>A , CM000664.1:g.27597945G>A	GRCh37
NC_000002.10:g.27451449G>A	NCBI36
NG_009305.1:g.380C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.699G>A MANE Select	ENSP00000233575.2:p.Glu233=
ENST00000233575.6:c.699G>A	ENSP00000233575.2:p.Glu233=
ENST00000427123.5:c.*509G>A	ENSP00000405399.1:n.*509G>A
ENST00000440760.5:c.*544G>A	ENSP00000399727.1:n.*544G>A
ENST00000453453.1:c.*226G>A	ENSP00000401922.1:n.*226G>A
ENST00000493711.1:n.416G>A
ENST00000494893.5:n.875G>A
ENST00000537606.5:c.624G>A	ENSP00000439208.1:p.Glu208=
NM_001267059.1:c.663G>A	NP_001253988.1:p.Glu221=
NM_001267060.1:c.624G>A	NP_001253989.1:p.Glu208=
NM_001267061.1:c.639G>A	NP_001253990.1:p.Glu213=
NM_014748.3:c.699G>A	NP_055563.1:p.Glu233=
NR_049782.1:n.1072G>A
NR_049783.1:n.1045G>A
NR_049784.1:n.1021G>A
NR_049785.1:n.954G>A
NR_049786.1:n.903G>A
NR_049787.1:n.754G>A
NR_049788.1:n.684G>A
XM_011533203.1:c.57G>A	XP_011531505.1:p.Glu19=
XM_011533203.2:c.57G>A	XP_011531505.1:p.Glu19=
XM_017005405.2:c.57G>A	XP_016860894.1:p.Glu19=
NM_014748.4:c.699G>A MANE Select	NP_055563.1:p.Glu233=
NM_001267059.2:c.663G>A	NP_001253988.1:p.Glu221=
NM_001267061.2:c.639G>A	NP_001253990.1:p.Glu213=
NR_049782.2:n.952G>A
NR_049783.2:n.925G>A
NR_049784.2:n.901G>A
NR_049785.2:n.834G>A
NR_049786.2:n.783G>A
NR_049787.2:n.634G>A
NR_049788.2:n.564G>A
NM_001267060.2:c.624G>A	NP_001253989.1:p.Glu208=