Canonical Allele Identifier: CA2576977418

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375062del , CM000664.2:g.27375062del	GRCh38
NC_000002.11:g.27597929del , CM000664.1:g.27597929del	GRCh37
NC_000002.10:g.27451433del	NCBI36
NG_009305.1:g.396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.683del MANE Select	ENSP00000233575.2:p.Thr228ArgfsTer?
ENST00000233575.6:c.683del	ENSP00000233575.2:p.Thr228ArgfsTer?
ENST00000427123.5:c.*493del	ENSP00000405399.1:n.*493del
ENST00000440760.5:c.*528del	ENSP00000399727.1:n.*528del
ENST00000453453.1:c.*210del	ENSP00000401922.1:n.*210del
ENST00000493711.1:n.400del
ENST00000494893.5:n.859del
ENST00000537606.5:c.608del	ENSP00000439208.1:p.Thr203ArgfsTer?
NM_001267059.1:c.647del	NP_001253988.1:p.Thr216ArgfsTer?
NM_001267060.1:c.608del	NP_001253989.1:p.Thr203ArgfsTer?
NM_001267061.1:c.623del	NP_001253990.1:p.Thr208ArgfsTer?
NM_014748.3:c.683del	NP_055563.1:p.Thr228ArgfsTer?
NR_049782.1:n.1056del
NR_049783.1:n.1029del
NR_049784.1:n.1005del
NR_049785.1:n.938del
NR_049786.1:n.887del
NR_049787.1:n.738del
NR_049788.1:n.668del
XM_011533203.1:c.41del	XP_011531505.1:p.Thr14ArgfsTer?
XM_011533203.2:c.41del	XP_011531505.1:p.Thr14ArgfsTer?
XM_017005405.2:c.41del	XP_016860894.1:p.Thr14ArgfsTer?
NM_014748.4:c.683del MANE Select	NP_055563.1:p.Thr228ArgfsTer?
NM_001267059.2:c.647del	NP_001253988.1:p.Thr216ArgfsTer?
NM_001267061.2:c.623del	NP_001253990.1:p.Thr208ArgfsTer?
NR_049782.2:n.936del
NR_049783.2:n.909del
NR_049784.2:n.885del
NR_049785.2:n.818del
NR_049786.2:n.767del
NR_049787.2:n.618del
NR_049788.2:n.548del
NM_001267060.2:c.608del	NP_001253989.1:p.Thr203ArgfsTer?