Canonical Allele Identifier: CA425606893

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598417C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375550C>G , CM000664.2:g.27375550C>G	GRCh38
NC_000002.11:g.27598417C>G , CM000664.1:g.27598417C>G	GRCh37
NC_000002.10:g.27451921C>G	NCBI36
NG_028219.1:g.10195G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.819C>G MANE Select	ENSP00000233575.2:p.Arg273=
ENST00000233575.6:c.819C>G	ENSP00000233575.2:p.Arg273=
ENST00000427123.5:c.*629C>G	ENSP00000405399.1:n.*629C>G
ENST00000440760.5:c.*664C>G	ENSP00000399727.1:n.*664C>G
ENST00000453453.1:c.*346C>G	ENSP00000401922.1:n.*346C>G
ENST00000493711.1:n.536C>G
ENST00000537606.5:c.744C>G	ENSP00000439208.1:p.Arg248=
NM_001267059.1:c.783C>G	NP_001253988.1:p.Arg261=
NM_001267060.1:c.744C>G	NP_001253989.1:p.Arg248=
NM_001267061.1:c.759C>G	NP_001253990.1:p.Arg253=
NM_014748.3:c.819C>G	NP_055563.1:p.Arg273=
NR_049782.1:n.1192C>G
NR_049783.1:n.1165C>G
NR_049784.1:n.1141C>G
NR_049785.1:n.1074C>G
NR_049786.1:n.1023C>G
NR_049787.1:n.874C>G
NR_049788.1:n.804C>G
XM_011533203.1:c.177C>G	XP_011531505.1:p.Arg59=
XM_011533203.2:c.177C>G	XP_011531505.1:p.Arg59=
XM_017005405.2:c.177C>G	XP_016860894.1:p.Arg59=
NM_014748.4:c.819C>G MANE Select	NP_055563.1:p.Arg273=
NM_001267059.2:c.783C>G	NP_001253988.1:p.Arg261=
NM_001267061.2:c.759C>G	NP_001253990.1:p.Arg253=
NR_049782.2:n.1072C>G
NR_049783.2:n.1045C>G
NR_049784.2:n.1021C>G
NR_049785.2:n.954C>G
NR_049786.2:n.903C>G
NR_049787.2:n.754C>G
NR_049788.2:n.684C>G
NM_001267060.2:c.744C>G	NP_001253989.1:p.Arg248=