Canonical Allele Identifier: CA346209686

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597946C>G (hg19) ; chr2:g.27375079C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375079C>G , CM000664.2:g.27375079C>G	GRCh38
NC_000002.11:g.27597946C>G , CM000664.1:g.27597946C>G	GRCh37
NC_000002.10:g.27451450C>G	NCBI36
NG_009305.1:g.379G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.700C>G MANE Select	ENSP00000233575.2:p.Arg234Gly
ENST00000233575.6:c.700C>G	ENSP00000233575.2:p.Arg234Gly
ENST00000427123.5:c.*510C>G	ENSP00000405399.1:n.*510C>G
ENST00000440760.5:c.*545C>G	ENSP00000399727.1:n.*545C>G
ENST00000453453.1:c.*227C>G	ENSP00000401922.1:n.*227C>G
ENST00000493711.1:n.417C>G
ENST00000494893.5:n.876C>G
ENST00000537606.5:c.625C>G	ENSP00000439208.1:p.Arg209Gly
NM_001267059.1:c.664C>G	NP_001253988.1:p.Arg222Gly
NM_001267060.1:c.625C>G	NP_001253989.1:p.Arg209Gly
NM_001267061.1:c.640C>G	NP_001253990.1:p.Arg214Gly
NM_014748.3:c.700C>G	NP_055563.1:p.Arg234Gly
NR_049782.1:n.1073C>G
NR_049783.1:n.1046C>G
NR_049784.1:n.1022C>G
NR_049785.1:n.955C>G
NR_049786.1:n.904C>G
NR_049787.1:n.755C>G
NR_049788.1:n.685C>G
XM_011533203.1:c.58C>G	XP_011531505.1:p.Arg20Gly
XM_011533203.2:c.58C>G	XP_011531505.1:p.Arg20Gly
XM_017005405.2:c.58C>G	XP_016860894.1:p.Arg20Gly
NM_014748.4:c.700C>G MANE Select	NP_055563.1:p.Arg234Gly
NM_001267059.2:c.664C>G	NP_001253988.1:p.Arg222Gly
NM_001267061.2:c.640C>G	NP_001253990.1:p.Arg214Gly
NR_049782.2:n.953C>G
NR_049783.2:n.926C>G
NR_049784.2:n.902C>G
NR_049785.2:n.835C>G
NR_049786.2:n.784C>G
NR_049787.2:n.635C>G
NR_049788.2:n.565C>G
NM_001267060.2:c.625C>G	NP_001253989.1:p.Arg209Gly