Canonical Allele Identifier: CA346209762

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597982C>G (hg19) ; chr2:g.27375115C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375115C>G , CM000664.2:g.27375115C>G	GRCh38
NC_000002.11:g.27597982C>G , CM000664.1:g.27597982C>G	GRCh37
NC_000002.10:g.27451486C>G	NCBI36
NG_009305.1:g.343G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.736C>G MANE Select	ENSP00000233575.2:p.Gln246Glu
ENST00000233575.6:c.736C>G	ENSP00000233575.2:p.Gln246Glu
ENST00000427123.5:c.*546C>G	ENSP00000405399.1:n.*546C>G
ENST00000440760.5:c.*581C>G	ENSP00000399727.1:n.*581C>G
ENST00000453453.1:c.*263C>G	ENSP00000401922.1:n.*263C>G
ENST00000493711.1:n.453C>G
ENST00000494893.5:n.912C>G
ENST00000537606.5:c.661C>G	ENSP00000439208.1:p.Gln221Glu
NM_001267059.1:c.700C>G	NP_001253988.1:p.Gln234Glu
NM_001267060.1:c.661C>G	NP_001253989.1:p.Gln221Glu
NM_001267061.1:c.676C>G	NP_001253990.1:p.Gln226Glu
NM_014748.3:c.736C>G	NP_055563.1:p.Gln246Glu
NR_049782.1:n.1109C>G
NR_049783.1:n.1082C>G
NR_049784.1:n.1058C>G
NR_049785.1:n.991C>G
NR_049786.1:n.940C>G
NR_049787.1:n.791C>G
NR_049788.1:n.721C>G
XM_011533203.1:c.94C>G	XP_011531505.1:p.Gln32Glu
XM_011533203.2:c.94C>G	XP_011531505.1:p.Gln32Glu
XM_017005405.2:c.94C>G	XP_016860894.1:p.Gln32Glu
NM_014748.4:c.736C>G MANE Select	NP_055563.1:p.Gln246Glu
NM_001267059.2:c.700C>G	NP_001253988.1:p.Gln234Glu
NM_001267061.2:c.676C>G	NP_001253990.1:p.Gln226Glu
NR_049782.2:n.989C>G
NR_049783.2:n.962C>G
NR_049784.2:n.938C>G
NR_049785.2:n.871C>G
NR_049786.2:n.820C>G
NR_049787.2:n.671C>G
NR_049788.2:n.601C>G
NM_001267060.2:c.661C>G	NP_001253989.1:p.Gln221Glu