Canonical Allele Identifier: CA346209726

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27597965C>T (hg19) ; chr2:g.27375098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375098C>T , CM000664.2:g.27375098C>T	GRCh38
NC_000002.11:g.27597965C>T , CM000664.1:g.27597965C>T	GRCh37
NC_000002.10:g.27451469C>T	NCBI36
NG_009305.1:g.360G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.719C>T MANE Select	ENSP00000233575.2:p.Thr240Ile
ENST00000233575.6:c.719C>T	ENSP00000233575.2:p.Thr240Ile
ENST00000427123.5:c.*529C>T	ENSP00000405399.1:n.*529C>T
ENST00000440760.5:c.*564C>T	ENSP00000399727.1:n.*564C>T
ENST00000453453.1:c.*246C>T	ENSP00000401922.1:n.*246C>T
ENST00000493711.1:n.436C>T
ENST00000494893.5:n.895C>T
ENST00000537606.5:c.644C>T	ENSP00000439208.1:p.Thr215Ile
NM_001267059.1:c.683C>T	NP_001253988.1:p.Thr228Ile
NM_001267060.1:c.644C>T	NP_001253989.1:p.Thr215Ile
NM_001267061.1:c.659C>T	NP_001253990.1:p.Thr220Ile
NM_014748.3:c.719C>T	NP_055563.1:p.Thr240Ile
NR_049782.1:n.1092C>T
NR_049783.1:n.1065C>T
NR_049784.1:n.1041C>T
NR_049785.1:n.974C>T
NR_049786.1:n.923C>T
NR_049787.1:n.774C>T
NR_049788.1:n.704C>T
XM_011533203.1:c.77C>T	XP_011531505.1:p.Thr26Ile
XM_011533203.2:c.77C>T	XP_011531505.1:p.Thr26Ile
XM_017005405.2:c.77C>T	XP_016860894.1:p.Thr26Ile
NM_014748.4:c.719C>T MANE Select	NP_055563.1:p.Thr240Ile
NM_001267059.2:c.683C>T	NP_001253988.1:p.Thr228Ile
NM_001267061.2:c.659C>T	NP_001253990.1:p.Thr220Ile
NR_049782.2:n.972C>T
NR_049783.2:n.945C>T
NR_049784.2:n.921C>T
NR_049785.2:n.854C>T
NR_049786.2:n.803C>T
NR_049787.2:n.654C>T
NR_049788.2:n.584C>T
NM_001267060.2:c.644C>T	NP_001253989.1:p.Thr215Ile