Canonical Allele Identifier: CA1028673278

Gene: SNX17

Linked Data

• dbSNP Id: rs1683089353
• gnomAD v3: 2-27375396-C-CT
• gnomAD v4: 2-27375396-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375397dup , CM000664.2:g.27375397dup	GRCh38
NC_000002.11:g.27598264dup , CM000664.1:g.27598264dup	GRCh37
NC_000002.10:g.27451768dup	NCBI36
NG_009305.1:g.61dup
NG_028219.1:g.10348dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-109dup MANE Select	ENSP00000233575.2:n.775-109dup
ENST00000233575.6:c.775-109dup	ENSP00000233575.2:n.775-109dup
ENST00000427123.5:c.*585-109dup	ENSP00000405399.1:n.*585-109dup
ENST00000440760.5:c.*620-109dup	ENSP00000399727.1:n.*620-109dup
ENST00000453453.1:c.*302-109dup	ENSP00000401922.1:n.*302-109dup
ENST00000493711.1:n.492-109dup
ENST00000494893.5:n.951-109dup
ENST00000537606.5:c.700-109dup	ENSP00000439208.1:n.700-109dup
NM_001267059.1:c.739-109dup	NP_001253988.1:n.739-109dup
NM_001267060.1:c.700-109dup	NP_001253989.1:n.700-109dup
NM_001267061.1:c.715-109dup	NP_001253990.1:n.715-109dup
NM_014748.3:c.775-109dup	NP_055563.1:n.775-109dup
NR_049782.1:n.1148-109dup
NR_049783.1:n.1121-109dup
NR_049784.1:n.1097-109dup
NR_049785.1:n.1030-109dup
NR_049786.1:n.979-109dup
NR_049787.1:n.830-109dup
NR_049788.1:n.760-109dup
XM_011533203.1:c.133-109dup	XP_011531505.1:n.133-109dup
XM_011533203.2:c.133-109dup	XP_011531505.1:n.133-109dup
XM_017005405.2:c.133-109dup	XP_016860894.1:n.133-109dup
NM_014748.4:c.775-109dup MANE Select	NP_055563.1:n.775-109dup
NM_001267059.2:c.739-109dup	NP_001253988.1:n.739-109dup
NM_001267061.2:c.715-109dup	NP_001253990.1:n.715-109dup
NR_049782.2:n.1028-109dup
NR_049783.2:n.1001-109dup
NR_049784.2:n.977-109dup
NR_049785.2:n.910-109dup
NR_049786.2:n.859-109dup
NR_049787.2:n.710-109dup
NR_049788.2:n.640-109dup
NM_001267060.2:c.700-109dup	NP_001253989.1:n.700-109dup