Canonical Allele Identifier: CA346210036

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598397C>G (hg19) ; chr2:g.27375530C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375530C>G , CM000664.2:g.27375530C>G	GRCh38
NC_000002.11:g.27598397C>G , CM000664.1:g.27598397C>G	GRCh37
NC_000002.10:g.27451901C>G	NCBI36
NG_028219.1:g.10215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.799C>G MANE Select	ENSP00000233575.2:p.Arg267Gly
ENST00000233575.6:c.799C>G	ENSP00000233575.2:p.Arg267Gly
ENST00000427123.5:c.*609C>G	ENSP00000405399.1:n.*609C>G
ENST00000440760.5:c.*644C>G	ENSP00000399727.1:n.*644C>G
ENST00000453453.1:c.*326C>G	ENSP00000401922.1:n.*326C>G
ENST00000493711.1:n.516C>G
ENST00000537606.5:c.724C>G	ENSP00000439208.1:p.Arg242Gly
NM_001267059.1:c.763C>G	NP_001253988.1:p.Arg255Gly
NM_001267060.1:c.724C>G	NP_001253989.1:p.Arg242Gly
NM_001267061.1:c.739C>G	NP_001253990.1:p.Arg247Gly
NM_014748.3:c.799C>G	NP_055563.1:p.Arg267Gly
NR_049782.1:n.1172C>G
NR_049783.1:n.1145C>G
NR_049784.1:n.1121C>G
NR_049785.1:n.1054C>G
NR_049786.1:n.1003C>G
NR_049787.1:n.854C>G
NR_049788.1:n.784C>G
XM_011533203.1:c.157C>G	XP_011531505.1:p.Arg53Gly
XM_011533203.2:c.157C>G	XP_011531505.1:p.Arg53Gly
XM_017005405.2:c.157C>G	XP_016860894.1:p.Arg53Gly
NM_014748.4:c.799C>G MANE Select	NP_055563.1:p.Arg267Gly
NM_001267059.2:c.763C>G	NP_001253988.1:p.Arg255Gly
NM_001267061.2:c.739C>G	NP_001253990.1:p.Arg247Gly
NR_049782.2:n.1052C>G
NR_049783.2:n.1025C>G
NR_049784.2:n.1001C>G
NR_049785.2:n.934C>G
NR_049786.2:n.883C>G
NR_049787.2:n.734C>G
NR_049788.2:n.664C>G
NM_001267060.2:c.724C>G	NP_001253989.1:p.Arg242Gly