Canonical Allele Identifier: CA346209715

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597961G>A (hg19) ; chr2:g.27375094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375094G>A , CM000664.2:g.27375094G>A	GRCh38
NC_000002.11:g.27597961G>A , CM000664.1:g.27597961G>A	GRCh37
NC_000002.10:g.27451465G>A	NCBI36
NG_009305.1:g.364C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.715G>A MANE Select	ENSP00000233575.2:p.Val239Ile
ENST00000233575.6:c.715G>A	ENSP00000233575.2:p.Val239Ile
ENST00000427123.5:c.*525G>A	ENSP00000405399.1:n.*525G>A
ENST00000440760.5:c.*560G>A	ENSP00000399727.1:n.*560G>A
ENST00000453453.1:c.*242G>A	ENSP00000401922.1:n.*242G>A
ENST00000493711.1:n.432G>A
ENST00000494893.5:n.891G>A
ENST00000537606.5:c.640G>A	ENSP00000439208.1:p.Val214Ile
NM_001267059.1:c.679G>A	NP_001253988.1:p.Val227Ile
NM_001267060.1:c.640G>A	NP_001253989.1:p.Val214Ile
NM_001267061.1:c.655G>A	NP_001253990.1:p.Val219Ile
NM_014748.3:c.715G>A	NP_055563.1:p.Val239Ile
NR_049782.1:n.1088G>A
NR_049783.1:n.1061G>A
NR_049784.1:n.1037G>A
NR_049785.1:n.970G>A
NR_049786.1:n.919G>A
NR_049787.1:n.770G>A
NR_049788.1:n.700G>A
XM_011533203.1:c.73G>A	XP_011531505.1:p.Val25Ile
XM_011533203.2:c.73G>A	XP_011531505.1:p.Val25Ile
XM_017005405.2:c.73G>A	XP_016860894.1:p.Val25Ile
NM_014748.4:c.715G>A MANE Select	NP_055563.1:p.Val239Ile
NM_001267059.2:c.679G>A	NP_001253988.1:p.Val227Ile
NM_001267061.2:c.655G>A	NP_001253990.1:p.Val219Ile
NR_049782.2:n.968G>A
NR_049783.2:n.941G>A
NR_049784.2:n.917G>A
NR_049785.2:n.850G>A
NR_049786.2:n.799G>A
NR_049787.2:n.650G>A
NR_049788.2:n.580G>A
NM_001267060.2:c.640G>A	NP_001253989.1:p.Val214Ile