Canonical Allele Identifier: CA2658341358

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375072-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375073dup , CM000664.2:g.27375073dup	GRCh38
NC_000002.11:g.27597940dup , CM000664.1:g.27597940dup	GRCh37
NC_000002.10:g.27451444dup	NCBI36
NG_009305.1:g.385dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.694dup MANE Select	ENSP00000233575.2:p.Ile232AsnfsTer2
ENST00000233575.6:c.694dup	ENSP00000233575.2:p.Ile232AsnfsTer2
ENST00000427123.5:c.*504dup	ENSP00000405399.1:n.*504dup
ENST00000440760.5:c.*539dup	ENSP00000399727.1:n.*539dup
ENST00000453453.1:c.*221dup	ENSP00000401922.1:n.*221dup
ENST00000493711.1:n.411dup
ENST00000494893.5:n.870dup
ENST00000537606.5:c.619dup	ENSP00000439208.1:p.Ile207AsnfsTer2
NM_001267059.1:c.658dup	NP_001253988.1:p.Ile220AsnfsTer2
NM_001267060.1:c.619dup	NP_001253989.1:p.Ile207AsnfsTer2
NM_001267061.1:c.634dup	NP_001253990.1:p.Ile212AsnfsTer2
NM_014748.3:c.694dup	NP_055563.1:p.Ile232AsnfsTer2
NR_049782.1:n.1067dup
NR_049783.1:n.1040dup
NR_049784.1:n.1016dup
NR_049785.1:n.949dup
NR_049786.1:n.898dup
NR_049787.1:n.749dup
NR_049788.1:n.679dup
XM_011533203.1:c.52dup	XP_011531505.1:p.Ile18AsnfsTer2
XM_011533203.2:c.52dup	XP_011531505.1:p.Ile18AsnfsTer2
XM_017005405.2:c.52dup	XP_016860894.1:p.Ile18AsnfsTer2
NM_014748.4:c.694dup MANE Select	NP_055563.1:p.Ile232AsnfsTer2
NM_001267059.2:c.658dup	NP_001253988.1:p.Ile220AsnfsTer2
NM_001267061.2:c.634dup	NP_001253990.1:p.Ile212AsnfsTer2
NR_049782.2:n.947dup
NR_049783.2:n.920dup
NR_049784.2:n.896dup
NR_049785.2:n.829dup
NR_049786.2:n.778dup
NR_049787.2:n.629dup
NR_049788.2:n.559dup
NM_001267060.2:c.619dup	NP_001253989.1:p.Ile207AsnfsTer2