Canonical Allele Identifier: CA346209718

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597962T>G (hg19) ; chr2:g.27375095T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375095T>G , CM000664.2:g.27375095T>G	GRCh38
NC_000002.11:g.27597962T>G , CM000664.1:g.27597962T>G	GRCh37
NC_000002.10:g.27451466T>G	NCBI36
NG_009305.1:g.363A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.716T>G MANE Select	ENSP00000233575.2:p.Val239Gly
ENST00000233575.6:c.716T>G	ENSP00000233575.2:p.Val239Gly
ENST00000427123.5:c.*526T>G	ENSP00000405399.1:n.*526T>G
ENST00000440760.5:c.*561T>G	ENSP00000399727.1:n.*561T>G
ENST00000453453.1:c.*243T>G	ENSP00000401922.1:n.*243T>G
ENST00000493711.1:n.433T>G
ENST00000494893.5:n.892T>G
ENST00000537606.5:c.641T>G	ENSP00000439208.1:p.Val214Gly
NM_001267059.1:c.680T>G	NP_001253988.1:p.Val227Gly
NM_001267060.1:c.641T>G	NP_001253989.1:p.Val214Gly
NM_001267061.1:c.656T>G	NP_001253990.1:p.Val219Gly
NM_014748.3:c.716T>G	NP_055563.1:p.Val239Gly
NR_049782.1:n.1089T>G
NR_049783.1:n.1062T>G
NR_049784.1:n.1038T>G
NR_049785.1:n.971T>G
NR_049786.1:n.920T>G
NR_049787.1:n.771T>G
NR_049788.1:n.701T>G
XM_011533203.1:c.74T>G	XP_011531505.1:p.Val25Gly
XM_011533203.2:c.74T>G	XP_011531505.1:p.Val25Gly
XM_017005405.2:c.74T>G	XP_016860894.1:p.Val25Gly
NM_014748.4:c.716T>G MANE Select	NP_055563.1:p.Val239Gly
NM_001267059.2:c.680T>G	NP_001253988.1:p.Val227Gly
NM_001267061.2:c.656T>G	NP_001253990.1:p.Val219Gly
NR_049782.2:n.969T>G
NR_049783.2:n.942T>G
NR_049784.2:n.918T>G
NR_049785.2:n.851T>G
NR_049786.2:n.800T>G
NR_049787.2:n.651T>G
NR_049788.2:n.581T>G
NM_001267060.2:c.641T>G	NP_001253989.1:p.Val214Gly