Canonical Allele Identifier: CA425606871

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598408C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375541C>A , CM000664.2:g.27375541C>A	GRCh38
NC_000002.11:g.27598408C>A , CM000664.1:g.27598408C>A	GRCh37
NC_000002.10:g.27451912C>A	NCBI36
NG_028219.1:g.10204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.810C>A MANE Select	ENSP00000233575.2:p.Gly270=
ENST00000233575.6:c.810C>A	ENSP00000233575.2:p.Gly270=
ENST00000427123.5:c.*620C>A	ENSP00000405399.1:n.*620C>A
ENST00000440760.5:c.*655C>A	ENSP00000399727.1:n.*655C>A
ENST00000453453.1:c.*337C>A	ENSP00000401922.1:n.*337C>A
ENST00000493711.1:n.527C>A
ENST00000537606.5:c.735C>A	ENSP00000439208.1:p.Gly245=
NM_001267059.1:c.774C>A	NP_001253988.1:p.Gly258=
NM_001267060.1:c.735C>A	NP_001253989.1:p.Gly245=
NM_001267061.1:c.750C>A	NP_001253990.1:p.Gly250=
NM_014748.3:c.810C>A	NP_055563.1:p.Gly270=
NR_049782.1:n.1183C>A
NR_049783.1:n.1156C>A
NR_049784.1:n.1132C>A
NR_049785.1:n.1065C>A
NR_049786.1:n.1014C>A
NR_049787.1:n.865C>A
NR_049788.1:n.795C>A
XM_011533203.1:c.168C>A	XP_011531505.1:p.Gly56=
XM_011533203.2:c.168C>A	XP_011531505.1:p.Gly56=
XM_017005405.2:c.168C>A	XP_016860894.1:p.Gly56=
NM_014748.4:c.810C>A MANE Select	NP_055563.1:p.Gly270=
NM_001267059.2:c.774C>A	NP_001253988.1:p.Gly258=
NM_001267061.2:c.750C>A	NP_001253990.1:p.Gly250=
NR_049782.2:n.1063C>A
NR_049783.2:n.1036C>A
NR_049784.2:n.1012C>A
NR_049785.2:n.945C>A
NR_049786.2:n.894C>A
NR_049787.2:n.745C>A
NR_049788.2:n.675C>A
NM_001267060.2:c.735C>A	NP_001253989.1:p.Gly245=