Canonical Allele Identifier: CA1577428

Gene: SNX17

Linked Data

• dbSNP Id: rs773177495
• ExAC: 2:27598354 T / C
• gnomAD v2: 2-27598354-T-C
• gnomAD v3: 2-27375487-T-C
• gnomAD v4: 2-27375487-T-C
• MyVariant Identifiers: chr2:g.27598354T>C (hg19) ; chr2:g.27375487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375487T>C , CM000664.2:g.27375487T>C	GRCh38
NC_000002.11:g.27598354T>C , CM000664.1:g.27598354T>C	GRCh37
NC_000002.10:g.27451858T>C	NCBI36
NG_028219.1:g.10258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-19T>C MANE Select	ENSP00000233575.2:n.775-19T>C
ENST00000233575.6:c.775-19T>C	ENSP00000233575.2:n.775-19T>C
ENST00000427123.5:c.*585-19T>C	ENSP00000405399.1:n.*585-19T>C
ENST00000440760.5:c.*620-19T>C	ENSP00000399727.1:n.*620-19T>C
ENST00000453453.1:c.*302-19T>C	ENSP00000401922.1:n.*302-19T>C
ENST00000493711.1:n.492-19T>C
ENST00000494893.5:n.951-19T>C
ENST00000537606.5:c.700-19T>C	ENSP00000439208.1:n.700-19T>C
NM_001267059.1:c.739-19T>C	NP_001253988.1:n.739-19T>C
NM_001267060.1:c.700-19T>C	NP_001253989.1:n.700-19T>C
NM_001267061.1:c.715-19T>C	NP_001253990.1:n.715-19T>C
NM_014748.3:c.775-19T>C	NP_055563.1:n.775-19T>C
NR_049782.1:n.1148-19T>C
NR_049783.1:n.1121-19T>C
NR_049784.1:n.1097-19T>C
NR_049785.1:n.1030-19T>C
NR_049786.1:n.979-19T>C
NR_049787.1:n.830-19T>C
NR_049788.1:n.760-19T>C
XM_011533203.1:c.133-19T>C	XP_011531505.1:n.133-19T>C
XM_011533203.2:c.133-19T>C	XP_011531505.1:n.133-19T>C
XM_017005405.2:c.133-19T>C	XP_016860894.1:n.133-19T>C
NM_014748.4:c.775-19T>C MANE Select	NP_055563.1:n.775-19T>C
NM_001267059.2:c.739-19T>C	NP_001253988.1:n.739-19T>C
NM_001267061.2:c.715-19T>C	NP_001253990.1:n.715-19T>C
NR_049782.2:n.1028-19T>C
NR_049783.2:n.1001-19T>C
NR_049784.2:n.977-19T>C
NR_049785.2:n.910-19T>C
NR_049786.2:n.859-19T>C
NR_049787.2:n.710-19T>C
NR_049788.2:n.640-19T>C
NM_001267060.2:c.700-19T>C	NP_001253989.1:n.700-19T>C