Canonical Allele Identifier: CA346209822

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598009T>C (hg19) ; chr2:g.27375142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375142T>C , CM000664.2:g.27375142T>C	GRCh38
NC_000002.11:g.27598009T>C , CM000664.1:g.27598009T>C	GRCh37
NC_000002.10:g.27451513T>C	NCBI36
NG_009305.1:g.316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.763T>C MANE Select	ENSP00000233575.2:p.Ser255Pro
ENST00000233575.6:c.763T>C	ENSP00000233575.2:p.Ser255Pro
ENST00000427123.5:c.*573T>C	ENSP00000405399.1:n.*573T>C
ENST00000440760.5:c.*608T>C	ENSP00000399727.1:n.*608T>C
ENST00000453453.1:c.*290T>C	ENSP00000401922.1:n.*290T>C
ENST00000493711.1:n.480T>C
ENST00000494893.5:n.939T>C
ENST00000537606.5:c.688T>C	ENSP00000439208.1:p.Ser230Pro
NM_001267059.1:c.727T>C	NP_001253988.1:p.Ser243Pro
NM_001267060.1:c.688T>C	NP_001253989.1:p.Ser230Pro
NM_001267061.1:c.703T>C	NP_001253990.1:p.Ser235Pro
NM_014748.3:c.763T>C	NP_055563.1:p.Ser255Pro
NR_049782.1:n.1136T>C
NR_049783.1:n.1109T>C
NR_049784.1:n.1085T>C
NR_049785.1:n.1018T>C
NR_049786.1:n.967T>C
NR_049787.1:n.818T>C
NR_049788.1:n.748T>C
XM_011533203.1:c.121T>C	XP_011531505.1:p.Ser41Pro
XM_011533203.2:c.121T>C	XP_011531505.1:p.Ser41Pro
XM_017005405.2:c.121T>C	XP_016860894.1:p.Ser41Pro
NM_014748.4:c.763T>C MANE Select	NP_055563.1:p.Ser255Pro
NM_001267059.2:c.727T>C	NP_001253988.1:p.Ser243Pro
NM_001267061.2:c.703T>C	NP_001253990.1:p.Ser235Pro
NR_049782.2:n.1016T>C
NR_049783.2:n.989T>C
NR_049784.2:n.965T>C
NR_049785.2:n.898T>C
NR_049786.2:n.847T>C
NR_049787.2:n.698T>C
NR_049788.2:n.628T>C
NM_001267060.2:c.688T>C	NP_001253989.1:p.Ser230Pro