Canonical Allele Identifier: CA2658341792

Gene: SNX17

Linked Data

• gnomAD v4: 2-27375450-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375451del , CM000664.2:g.27375451del	GRCh38
NC_000002.11:g.27598318del , CM000664.1:g.27598318del	GRCh37
NC_000002.10:g.27451822del	NCBI36
NG_009305.1:g.7del
NG_028219.1:g.10294del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.775-55del MANE Select	ENSP00000233575.2:n.775-55del
ENST00000233575.6:c.775-55del	ENSP00000233575.2:n.775-55del
ENST00000427123.5:c.*585-55del	ENSP00000405399.1:n.*585-55del
ENST00000440760.5:c.*620-55del	ENSP00000399727.1:n.*620-55del
ENST00000453453.1:c.*302-55del	ENSP00000401922.1:n.*302-55del
ENST00000493711.1:n.492-55del
ENST00000494893.5:n.951-55del
ENST00000537606.5:c.700-55del	ENSP00000439208.1:n.700-55del
NM_001267059.1:c.739-55del	NP_001253988.1:n.739-55del
NM_001267060.1:c.700-55del	NP_001253989.1:n.700-55del
NM_001267061.1:c.715-55del	NP_001253990.1:n.715-55del
NM_014748.3:c.775-55del	NP_055563.1:n.775-55del
NR_049782.1:n.1148-55del
NR_049783.1:n.1121-55del
NR_049784.1:n.1097-55del
NR_049785.1:n.1030-55del
NR_049786.1:n.979-55del
NR_049787.1:n.830-55del
NR_049788.1:n.760-55del
XM_011533203.1:c.133-55del	XP_011531505.1:n.133-55del
XM_011533203.2:c.133-55del	XP_011531505.1:n.133-55del
XM_017005405.2:c.133-55del	XP_016860894.1:n.133-55del
NM_014748.4:c.775-55del MANE Select	NP_055563.1:n.775-55del
NM_001267059.2:c.739-55del	NP_001253988.1:n.739-55del
NM_001267061.2:c.715-55del	NP_001253990.1:n.715-55del
NR_049782.2:n.1028-55del
NR_049783.2:n.1001-55del
NR_049784.2:n.977-55del
NR_049785.2:n.910-55del
NR_049786.2:n.859-55del
NR_049787.2:n.710-55del
NR_049788.2:n.640-55del
NM_001267060.2:c.700-55del	NP_001253989.1:n.700-55del