Canonical Allele Identifier: CA346210044

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598400C>A (hg19) ; chr2:g.27375533C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375533C>A , CM000664.2:g.27375533C>A	GRCh38
NC_000002.11:g.27598400C>A , CM000664.1:g.27598400C>A	GRCh37
NC_000002.10:g.27451904C>A	NCBI36
NG_028219.1:g.10212G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.802C>A MANE Select	ENSP00000233575.2:p.His268Asn
ENST00000233575.6:c.802C>A	ENSP00000233575.2:p.His268Asn
ENST00000427123.5:c.*612C>A	ENSP00000405399.1:n.*612C>A
ENST00000440760.5:c.*647C>A	ENSP00000399727.1:n.*647C>A
ENST00000453453.1:c.*329C>A	ENSP00000401922.1:n.*329C>A
ENST00000493711.1:n.519C>A
ENST00000537606.5:c.727C>A	ENSP00000439208.1:p.His243Asn
NM_001267059.1:c.766C>A	NP_001253988.1:p.His256Asn
NM_001267060.1:c.727C>A	NP_001253989.1:p.His243Asn
NM_001267061.1:c.742C>A	NP_001253990.1:p.His248Asn
NM_014748.3:c.802C>A	NP_055563.1:p.His268Asn
NR_049782.1:n.1175C>A
NR_049783.1:n.1148C>A
NR_049784.1:n.1124C>A
NR_049785.1:n.1057C>A
NR_049786.1:n.1006C>A
NR_049787.1:n.857C>A
NR_049788.1:n.787C>A
XM_011533203.1:c.160C>A	XP_011531505.1:p.His54Asn
XM_011533203.2:c.160C>A	XP_011531505.1:p.His54Asn
XM_017005405.2:c.160C>A	XP_016860894.1:p.His54Asn
NM_014748.4:c.802C>A MANE Select	NP_055563.1:p.His268Asn
NM_001267059.2:c.766C>A	NP_001253988.1:p.His256Asn
NM_001267061.2:c.742C>A	NP_001253990.1:p.His248Asn
NR_049782.2:n.1055C>A
NR_049783.2:n.1028C>A
NR_049784.2:n.1004C>A
NR_049785.2:n.937C>A
NR_049786.2:n.886C>A
NR_049787.2:n.737C>A
NR_049788.2:n.667C>A
NM_001267060.2:c.727C>A	NP_001253989.1:p.His243Asn