Canonical Allele Identifier: CA2658341692

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375392-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375392C>A , CM000664.2:g.27375392C>A	GRCh38
NC_000002.11:g.27598259C>A , CM000664.1:g.27598259C>A	GRCh37
NC_000002.10:g.27451763C>A	NCBI36
NG_009305.1:g.66G>T
NG_028219.1:g.10353G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-114C>A MANE Select	ENSP00000233575.2:n.775-114C>A
ENST00000233575.6:c.775-114C>A	ENSP00000233575.2:n.775-114C>A
ENST00000427123.5:c.*585-114C>A	ENSP00000405399.1:n.*585-114C>A
ENST00000440760.5:c.*620-114C>A	ENSP00000399727.1:n.*620-114C>A
ENST00000453453.1:c.*302-114C>A	ENSP00000401922.1:n.*302-114C>A
ENST00000493711.1:n.492-114C>A
ENST00000494893.5:n.951-114C>A
ENST00000537606.5:c.700-114C>A	ENSP00000439208.1:n.700-114C>A
NM_001267059.1:c.739-114C>A	NP_001253988.1:n.739-114C>A
NM_001267060.1:c.700-114C>A	NP_001253989.1:n.700-114C>A
NM_001267061.1:c.715-114C>A	NP_001253990.1:n.715-114C>A
NM_014748.3:c.775-114C>A	NP_055563.1:n.775-114C>A
NR_049782.1:n.1148-114C>A
NR_049783.1:n.1121-114C>A
NR_049784.1:n.1097-114C>A
NR_049785.1:n.1030-114C>A
NR_049786.1:n.979-114C>A
NR_049787.1:n.830-114C>A
NR_049788.1:n.760-114C>A
XM_011533203.1:c.133-114C>A	XP_011531505.1:n.133-114C>A
XM_011533203.2:c.133-114C>A	XP_011531505.1:n.133-114C>A
XM_017005405.2:c.133-114C>A	XP_016860894.1:n.133-114C>A
NM_014748.4:c.775-114C>A MANE Select	NP_055563.1:n.775-114C>A
NM_001267059.2:c.739-114C>A	NP_001253988.1:n.739-114C>A
NM_001267061.2:c.715-114C>A	NP_001253990.1:n.715-114C>A
NR_049782.2:n.1028-114C>A
NR_049783.2:n.1001-114C>A
NR_049784.2:n.977-114C>A
NR_049785.2:n.910-114C>A
NR_049786.2:n.859-114C>A
NR_049787.2:n.710-114C>A
NR_049788.2:n.640-114C>A
NM_001267060.2:c.700-114C>A	NP_001253989.1:n.700-114C>A