Canonical Allele Identifier: CA346209661

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597935C>A (hg19) ; chr2:g.27375068C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375068C>A , CM000664.2:g.27375068C>A	GRCh38
NC_000002.11:g.27597935C>A , CM000664.1:g.27597935C>A	GRCh37
NC_000002.10:g.27451439C>A	NCBI36
NG_009305.1:g.390G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.689C>A MANE Select	ENSP00000233575.2:p.Ser230Ter
ENST00000233575.6:c.689C>A	ENSP00000233575.2:p.Ser230Ter
ENST00000427123.5:c.*499C>A	ENSP00000405399.1:n.*499C>A
ENST00000440760.5:c.*534C>A	ENSP00000399727.1:n.*534C>A
ENST00000453453.1:c.*216C>A	ENSP00000401922.1:n.*216C>A
ENST00000493711.1:n.406C>A
ENST00000494893.5:n.865C>A
ENST00000537606.5:c.614C>A	ENSP00000439208.1:p.Ser205Ter
NM_001267059.1:c.653C>A	NP_001253988.1:p.Ser218Ter
NM_001267060.1:c.614C>A	NP_001253989.1:p.Ser205Ter
NM_001267061.1:c.629C>A	NP_001253990.1:p.Ser210Ter
NM_014748.3:c.689C>A	NP_055563.1:p.Ser230Ter
NR_049782.1:n.1062C>A
NR_049783.1:n.1035C>A
NR_049784.1:n.1011C>A
NR_049785.1:n.944C>A
NR_049786.1:n.893C>A
NR_049787.1:n.744C>A
NR_049788.1:n.674C>A
XM_011533203.1:c.47C>A	XP_011531505.1:p.Ser16Ter
XM_011533203.2:c.47C>A	XP_011531505.1:p.Ser16Ter
XM_017005405.2:c.47C>A	XP_016860894.1:p.Ser16Ter
NM_014748.4:c.689C>A MANE Select	NP_055563.1:p.Ser230Ter
NM_001267059.2:c.653C>A	NP_001253988.1:p.Ser218Ter
NM_001267061.2:c.629C>A	NP_001253990.1:p.Ser210Ter
NR_049782.2:n.942C>A
NR_049783.2:n.915C>A
NR_049784.2:n.891C>A
NR_049785.2:n.824C>A
NR_049786.2:n.773C>A
NR_049787.2:n.624C>A
NR_049788.2:n.554C>A
NM_001267060.2:c.614C>A	NP_001253989.1:p.Ser205Ter