Canonical Allele Identifier: CA425415817

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597999A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375132A>G , CM000664.2:g.27375132A>G	GRCh38
NC_000002.11:g.27597999A>G , CM000664.1:g.27597999A>G	GRCh37
NC_000002.10:g.27451503A>G	NCBI36
NG_009305.1:g.326T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.753A>G MANE Select	ENSP00000233575.2:p.Gln251=
ENST00000233575.6:c.753A>G	ENSP00000233575.2:p.Gln251=
ENST00000427123.5:c.*563A>G	ENSP00000405399.1:n.*563A>G
ENST00000440760.5:c.*598A>G	ENSP00000399727.1:n.*598A>G
ENST00000453453.1:c.*280A>G	ENSP00000401922.1:n.*280A>G
ENST00000493711.1:n.470A>G
ENST00000494893.5:n.929A>G
ENST00000537606.5:c.678A>G	ENSP00000439208.1:p.Gln226=
NM_001267059.1:c.717A>G	NP_001253988.1:p.Gln239=
NM_001267060.1:c.678A>G	NP_001253989.1:p.Gln226=
NM_001267061.1:c.693A>G	NP_001253990.1:p.Gln231=
NM_014748.3:c.753A>G	NP_055563.1:p.Gln251=
NR_049782.1:n.1126A>G
NR_049783.1:n.1099A>G
NR_049784.1:n.1075A>G
NR_049785.1:n.1008A>G
NR_049786.1:n.957A>G
NR_049787.1:n.808A>G
NR_049788.1:n.738A>G
XM_011533203.1:c.111A>G	XP_011531505.1:p.Gln37=
XM_011533203.2:c.111A>G	XP_011531505.1:p.Gln37=
XM_017005405.2:c.111A>G	XP_016860894.1:p.Gln37=
NM_014748.4:c.753A>G MANE Select	NP_055563.1:p.Gln251=
NM_001267059.2:c.717A>G	NP_001253988.1:p.Gln239=
NM_001267061.2:c.693A>G	NP_001253990.1:p.Gln231=
NR_049782.2:n.1006A>G
NR_049783.2:n.979A>G
NR_049784.2:n.955A>G
NR_049785.2:n.888A>G
NR_049786.2:n.837A>G
NR_049787.2:n.688A>G
NR_049788.2:n.618A>G
NM_001267060.2:c.678A>G	NP_001253989.1:p.Gln226=