Canonical Allele Identifier: CA1577385

Gene: SNX17

Linked Data

• dbSNP Id: rs760977171
• ExAC: 2:27597910 C / A
• gnomAD v2: 2-27597910-C-A
• gnomAD v4: 2-27375043-C-A
• MyVariant Identifiers: chr2:g.27597910C>A (hg19) ; chr2:g.27375043C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375043C>A , CM000664.2:g.27375043C>A	GRCh38
NC_000002.11:g.27597910C>A , CM000664.1:g.27597910C>A	GRCh37
NC_000002.10:g.27451414C>A	NCBI36
NG_009305.1:g.415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.682-18C>A MANE Select	ENSP00000233575.2:n.682-18C>A
ENST00000233575.6:c.682-18C>A	ENSP00000233575.2:n.682-18C>A
ENST00000427123.5:c.*492-18C>A	ENSP00000405399.1:n.*492-18C>A
ENST00000440760.5:c.*527-18C>A	ENSP00000399727.1:n.*527-18C>A
ENST00000453453.1:c.*209-18C>A	ENSP00000401922.1:n.*209-18C>A
ENST00000493711.1:n.381C>A
ENST00000494893.5:n.858-18C>A
ENST00000537606.5:c.607-18C>A	ENSP00000439208.1:n.607-18C>A
NM_001267059.1:c.646-18C>A	NP_001253988.1:n.646-18C>A
NM_001267060.1:c.607-18C>A	NP_001253989.1:n.607-18C>A
NM_001267061.1:c.622-18C>A	NP_001253990.1:n.622-18C>A
NM_014748.3:c.682-18C>A	NP_055563.1:n.682-18C>A
NR_049782.1:n.1055-18C>A
NR_049783.1:n.1028-18C>A
NR_049784.1:n.1004-18C>A
NR_049785.1:n.937-18C>A
NR_049786.1:n.886-18C>A
NR_049787.1:n.737-18C>A
NR_049788.1:n.667-18C>A
XM_011533203.1:c.40-18C>A	XP_011531505.1:n.40-18C>A
XM_011533203.2:c.40-18C>A	XP_011531505.1:n.40-18C>A
XM_017005405.2:c.40-18C>A	XP_016860894.1:n.40-18C>A
NM_014748.4:c.682-18C>A MANE Select	NP_055563.1:n.682-18C>A
NM_001267059.2:c.646-18C>A	NP_001253988.1:n.646-18C>A
NM_001267061.2:c.622-18C>A	NP_001253990.1:n.622-18C>A
NR_049782.2:n.935-18C>A
NR_049783.2:n.908-18C>A
NR_049784.2:n.884-18C>A
NR_049785.2:n.817-18C>A
NR_049786.2:n.766-18C>A
NR_049787.2:n.617-18C>A
NR_049788.2:n.547-18C>A
NM_001267060.2:c.607-18C>A	NP_001253989.1:n.607-18C>A