Canonical Allele Identifier: CA346209676

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597942T>G (hg19) ; chr2:g.27375075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375075T>G , CM000664.2:g.27375075T>G	GRCh38
NC_000002.11:g.27597942T>G , CM000664.1:g.27597942T>G	GRCh37
NC_000002.10:g.27451446T>G	NCBI36
NG_009305.1:g.383A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.696T>G MANE Select	ENSP00000233575.2:p.Ile232Met
ENST00000233575.6:c.696T>G	ENSP00000233575.2:p.Ile232Met
ENST00000427123.5:c.*506T>G	ENSP00000405399.1:n.*506T>G
ENST00000440760.5:c.*541T>G	ENSP00000399727.1:n.*541T>G
ENST00000453453.1:c.*223T>G	ENSP00000401922.1:n.*223T>G
ENST00000493711.1:n.413T>G
ENST00000494893.5:n.872T>G
ENST00000537606.5:c.621T>G	ENSP00000439208.1:p.Ile207Met
NM_001267059.1:c.660T>G	NP_001253988.1:p.Ile220Met
NM_001267060.1:c.621T>G	NP_001253989.1:p.Ile207Met
NM_001267061.1:c.636T>G	NP_001253990.1:p.Ile212Met
NM_014748.3:c.696T>G	NP_055563.1:p.Ile232Met
NR_049782.1:n.1069T>G
NR_049783.1:n.1042T>G
NR_049784.1:n.1018T>G
NR_049785.1:n.951T>G
NR_049786.1:n.900T>G
NR_049787.1:n.751T>G
NR_049788.1:n.681T>G
XM_011533203.1:c.54T>G	XP_011531505.1:p.Ile18Met
XM_011533203.2:c.54T>G	XP_011531505.1:p.Ile18Met
XM_017005405.2:c.54T>G	XP_016860894.1:p.Ile18Met
NM_014748.4:c.696T>G MANE Select	NP_055563.1:p.Ile232Met
NM_001267059.2:c.660T>G	NP_001253988.1:p.Ile220Met
NM_001267061.2:c.636T>G	NP_001253990.1:p.Ile212Met
NR_049782.2:n.949T>G
NR_049783.2:n.922T>G
NR_049784.2:n.898T>G
NR_049785.2:n.831T>G
NR_049786.2:n.780T>G
NR_049787.2:n.631T>G
NR_049788.2:n.561T>G
NM_001267060.2:c.621T>G	NP_001253989.1:p.Ile207Met