Canonical Allele Identifier: CA2658341620

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375362-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375362G>A , CM000664.2:g.27375362G>A	GRCh38
NC_000002.11:g.27598229G>A , CM000664.1:g.27598229G>A	GRCh37
NC_000002.10:g.27451733G>A	NCBI36
NG_009305.1:g.96C>T
NG_028219.1:g.10383C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-144G>A MANE Select	ENSP00000233575.2:n.775-144G>A
ENST00000233575.6:c.775-144G>A	ENSP00000233575.2:n.775-144G>A
ENST00000427123.5:c.*585-144G>A	ENSP00000405399.1:n.*585-144G>A
ENST00000440760.5:c.*620-144G>A	ENSP00000399727.1:n.*620-144G>A
ENST00000453453.1:c.*302-144G>A	ENSP00000401922.1:n.*302-144G>A
ENST00000493711.1:n.492-144G>A
ENST00000494893.5:n.951-144G>A
ENST00000537606.5:c.700-144G>A	ENSP00000439208.1:n.700-144G>A
NM_001267059.1:c.739-144G>A	NP_001253988.1:n.739-144G>A
NM_001267060.1:c.700-144G>A	NP_001253989.1:n.700-144G>A
NM_001267061.1:c.715-144G>A	NP_001253990.1:n.715-144G>A
NM_014748.3:c.775-144G>A	NP_055563.1:n.775-144G>A
NR_049782.1:n.1148-144G>A
NR_049783.1:n.1121-144G>A
NR_049784.1:n.1097-144G>A
NR_049785.1:n.1030-144G>A
NR_049786.1:n.979-144G>A
NR_049787.1:n.830-144G>A
NR_049788.1:n.760-144G>A
XM_011533203.1:c.133-144G>A	XP_011531505.1:n.133-144G>A
XM_011533203.2:c.133-144G>A	XP_011531505.1:n.133-144G>A
XM_017005405.2:c.133-144G>A	XP_016860894.1:n.133-144G>A
NM_014748.4:c.775-144G>A MANE Select	NP_055563.1:n.775-144G>A
NM_001267059.2:c.739-144G>A	NP_001253988.1:n.739-144G>A
NM_001267061.2:c.715-144G>A	NP_001253990.1:n.715-144G>A
NR_049782.2:n.1028-144G>A
NR_049783.2:n.1001-144G>A
NR_049784.2:n.977-144G>A
NR_049785.2:n.910-144G>A
NR_049786.2:n.859-144G>A
NR_049787.2:n.710-144G>A
NR_049788.2:n.640-144G>A
NM_001267060.2:c.700-144G>A	NP_001253989.1:n.700-144G>A