Canonical Allele Identifier: CA2576977453
Gene: SNX17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27375500_27375502del , CM000664.2:g.27375500_27375502del GRCh38
NC_000002.11:g.27598367_27598369del , CM000664.1:g.27598367_27598369del GRCh37
NC_000002.10:g.27451871_27451873del NCBI36
NG_028219.1:g.10245_10247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233575.7:c.775-6_775-4del MANE Select ENSP00000233575.2:n.775-6_775-4del
ENST00000233575.6:c.775-6_775-4del ENSP00000233575.2:n.775-6_775-4del
ENST00000427123.5:c.*585-6_*585-4del ENSP00000405399.1:n.*585-6_*585-4del
ENST00000440760.5:c.*620-6_*620-4del ENSP00000399727.1:n.*620-6_*620-4del
ENST00000453453.1:c.*302-6_*302-4del ENSP00000401922.1:n.*302-6_*302-4del
ENST00000493711.1:n.492-6_492-4del
ENST00000494893.5:n.951-6_951-4del
ENST00000537606.5:c.700-6_700-4del ENSP00000439208.1:n.700-6_700-4del
NM_001267059.1:c.739-6_739-4del NP_001253988.1:n.739-6_739-4del
NM_001267060.1:c.700-6_700-4del NP_001253989.1:n.700-6_700-4del
NM_001267061.1:c.715-6_715-4del NP_001253990.1:n.715-6_715-4del
NM_014748.3:c.775-6_775-4del NP_055563.1:n.775-6_775-4del
NR_049782.1:n.1148-6_1148-4del
NR_049783.1:n.1121-6_1121-4del
NR_049784.1:n.1097-6_1097-4del
NR_049785.1:n.1030-6_1030-4del
NR_049786.1:n.979-6_979-4del
NR_049787.1:n.830-6_830-4del
NR_049788.1:n.760-6_760-4del
XM_011533203.1:c.133-6_133-4del XP_011531505.1:n.133-6_133-4del
XM_011533203.2:c.133-6_133-4del XP_011531505.1:n.133-6_133-4del
XM_017005405.2:c.133-6_133-4del XP_016860894.1:n.133-6_133-4del
NM_014748.4:c.775-6_775-4del MANE Select NP_055563.1:n.775-6_775-4del
NM_001267059.2:c.739-6_739-4del NP_001253988.1:n.739-6_739-4del
NM_001267061.2:c.715-6_715-4del NP_001253990.1:n.715-6_715-4del
NR_049782.2:n.1028-6_1028-4del
NR_049783.2:n.1001-6_1001-4del
NR_049784.2:n.977-6_977-4del
NR_049785.2:n.910-6_910-4del
NR_049786.2:n.859-6_859-4del
NR_049787.2:n.710-6_710-4del
NR_049788.2:n.640-6_640-4del
NM_001267060.2:c.700-6_700-4del NP_001253989.1:n.700-6_700-4del