Canonical Allele Identifier: CA346209706

Gene: SNX17

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.710T>G MANE Select	ENSP00000233575.2:p.Ile237Ser
ENST00000233575.6:c.710T>G	ENSP00000233575.2:p.Ile237Ser
ENST00000427123.5:c.*520T>G	ENSP00000405399.1:n.*520T>G
ENST00000440760.5:c.*555T>G	ENSP00000399727.1:n.*555T>G
ENST00000453453.1:c.*237T>G	ENSP00000401922.1:n.*237T>G
ENST00000493711.1:n.427T>G
ENST00000494893.5:n.886T>G
ENST00000537606.5:c.635T>G	ENSP00000439208.1:p.Ile212Ser
NM_001267059.1:c.674T>G	NP_001253988.1:p.Ile225Ser
NM_001267060.1:c.635T>G	NP_001253989.1:p.Ile212Ser
NM_001267061.1:c.650T>G	NP_001253990.1:p.Ile217Ser
NM_014748.3:c.710T>G	NP_055563.1:p.Ile237Ser
NR_049782.1:n.1083T>G
NR_049783.1:n.1056T>G
NR_049784.1:n.1032T>G
NR_049785.1:n.965T>G
NR_049786.1:n.914T>G
NR_049787.1:n.765T>G
NR_049788.1:n.695T>G
XM_011533203.1:c.68T>G	XP_011531505.1:p.Ile23Ser
XM_011533203.2:c.68T>G	XP_011531505.1:p.Ile23Ser
XM_017005405.2:c.68T>G	XP_016860894.1:p.Ile23Ser
NM_014748.4:c.710T>G MANE Select	NP_055563.1:p.Ile237Ser
NM_001267059.2:c.674T>G	NP_001253988.1:p.Ile225Ser
NM_001267061.2:c.650T>G	NP_001253990.1:p.Ile217Ser
NR_049782.2:n.963T>G
NR_049783.2:n.936T>G
NR_049784.2:n.912T>G
NR_049785.2:n.845T>G
NR_049786.2:n.794T>G
NR_049787.2:n.645T>G
NR_049788.2:n.575T>G
NM_001267060.2:c.635T>G	NP_001253989.1:p.Ile212Ser