Canonical Allele Identifier: CA346209705

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597956T>A (hg19) ; chr2:g.27375089T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375089T>A , CM000664.2:g.27375089T>A	GRCh38
NC_000002.11:g.27597956T>A , CM000664.1:g.27597956T>A	GRCh37
NC_000002.10:g.27451460T>A	NCBI36
NG_009305.1:g.369A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.710T>A MANE Select	ENSP00000233575.2:p.Ile237Asn
ENST00000233575.6:c.710T>A	ENSP00000233575.2:p.Ile237Asn
ENST00000427123.5:c.*520T>A	ENSP00000405399.1:n.*520T>A
ENST00000440760.5:c.*555T>A	ENSP00000399727.1:n.*555T>A
ENST00000453453.1:c.*237T>A	ENSP00000401922.1:n.*237T>A
ENST00000493711.1:n.427T>A
ENST00000494893.5:n.886T>A
ENST00000537606.5:c.635T>A	ENSP00000439208.1:p.Ile212Asn
NM_001267059.1:c.674T>A	NP_001253988.1:p.Ile225Asn
NM_001267060.1:c.635T>A	NP_001253989.1:p.Ile212Asn
NM_001267061.1:c.650T>A	NP_001253990.1:p.Ile217Asn
NM_014748.3:c.710T>A	NP_055563.1:p.Ile237Asn
NR_049782.1:n.1083T>A
NR_049783.1:n.1056T>A
NR_049784.1:n.1032T>A
NR_049785.1:n.965T>A
NR_049786.1:n.914T>A
NR_049787.1:n.765T>A
NR_049788.1:n.695T>A
XM_011533203.1:c.68T>A	XP_011531505.1:p.Ile23Asn
XM_011533203.2:c.68T>A	XP_011531505.1:p.Ile23Asn
XM_017005405.2:c.68T>A	XP_016860894.1:p.Ile23Asn
NM_014748.4:c.710T>A MANE Select	NP_055563.1:p.Ile237Asn
NM_001267059.2:c.674T>A	NP_001253988.1:p.Ile225Asn
NM_001267061.2:c.650T>A	NP_001253990.1:p.Ile217Asn
NR_049782.2:n.963T>A
NR_049783.2:n.936T>A
NR_049784.2:n.912T>A
NR_049785.2:n.845T>A
NR_049786.2:n.794T>A
NR_049787.2:n.645T>A
NR_049788.2:n.575T>A
NM_001267060.2:c.635T>A	NP_001253989.1:p.Ile212Asn