Canonical Allele Identifier: CA346209655

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597932T>G (hg19) ; chr2:g.27375065T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375065T>G , CM000664.2:g.27375065T>G	GRCh38
NC_000002.11:g.27597932T>G , CM000664.1:g.27597932T>G	GRCh37
NC_000002.10:g.27451436T>G	NCBI36
NG_009305.1:g.393A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.686T>G MANE Select	ENSP00000233575.2:p.Val229Gly
ENST00000233575.6:c.686T>G	ENSP00000233575.2:p.Val229Gly
ENST00000427123.5:c.*496T>G	ENSP00000405399.1:n.*496T>G
ENST00000440760.5:c.*531T>G	ENSP00000399727.1:n.*531T>G
ENST00000453453.1:c.*213T>G	ENSP00000401922.1:n.*213T>G
ENST00000493711.1:n.403T>G
ENST00000494893.5:n.862T>G
ENST00000537606.5:c.611T>G	ENSP00000439208.1:p.Val204Gly
NM_001267059.1:c.650T>G	NP_001253988.1:p.Val217Gly
NM_001267060.1:c.611T>G	NP_001253989.1:p.Val204Gly
NM_001267061.1:c.626T>G	NP_001253990.1:p.Val209Gly
NM_014748.3:c.686T>G	NP_055563.1:p.Val229Gly
NR_049782.1:n.1059T>G
NR_049783.1:n.1032T>G
NR_049784.1:n.1008T>G
NR_049785.1:n.941T>G
NR_049786.1:n.890T>G
NR_049787.1:n.741T>G
NR_049788.1:n.671T>G
XM_011533203.1:c.44T>G	XP_011531505.1:p.Val15Gly
XM_011533203.2:c.44T>G	XP_011531505.1:p.Val15Gly
XM_017005405.2:c.44T>G	XP_016860894.1:p.Val15Gly
NM_014748.4:c.686T>G MANE Select	NP_055563.1:p.Val229Gly
NM_001267059.2:c.650T>G	NP_001253988.1:p.Val217Gly
NM_001267061.2:c.626T>G	NP_001253990.1:p.Val209Gly
NR_049782.2:n.939T>G
NR_049783.2:n.912T>G
NR_049784.2:n.888T>G
NR_049785.2:n.821T>G
NR_049786.2:n.770T>G
NR_049787.2:n.621T>G
NR_049788.2:n.551T>G
NM_001267060.2:c.611T>G	NP_001253989.1:p.Val204Gly