Canonical Allele Identifier: CA1240248131
Gene: SNX17 HGNC NCBI

Linked Data

dbSNP Id: rs1683049636

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27375211_27375226del , CM000664.2:g.27375211_27375226del GRCh38
NC_000002.11:g.27598078_27598093del , CM000664.1:g.27598078_27598093del GRCh37
NC_000002.10:g.27451582_27451597del NCBI36
NG_009305.1:g.234_249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233575.7:c.774+58_774+73del MANE Select ENSP00000233575.2:n.774+58_774+73del
ENST00000233575.6:c.774+58_774+73del ENSP00000233575.2:n.774+58_774+73del
ENST00000427123.5:c.*584+58_*584+73del ENSP00000405399.1:n.*584+58_*584+73del
ENST00000440760.5:c.*619+58_*619+73del ENSP00000399727.1:n.*619+58_*619+73del
ENST00000453453.1:c.*301+58_*301+73del ENSP00000401922.1:n.*301+58_*301+73del
ENST00000493711.1:n.491+58_491+73del
ENST00000494893.5:n.950+58_950+73del
ENST00000537606.5:c.699+58_699+73del ENSP00000439208.1:n.699+58_699+73del
NM_001267059.1:c.738+58_738+73del NP_001253988.1:n.738+58_738+73del
NM_001267060.1:c.699+58_699+73del NP_001253989.1:n.699+58_699+73del
NM_001267061.1:c.714+58_714+73del NP_001253990.1:n.714+58_714+73del
NM_014748.3:c.774+58_774+73del NP_055563.1:n.774+58_774+73del
NR_049782.1:n.1147+58_1147+73del
NR_049783.1:n.1120+58_1120+73del
NR_049784.1:n.1096+58_1096+73del
NR_049785.1:n.1029+58_1029+73del
NR_049786.1:n.978+58_978+73del
NR_049787.1:n.829+58_829+73del
NR_049788.1:n.759+58_759+73del
XM_011533203.1:c.132+58_132+73del XP_011531505.1:n.132+58_132+73del
XM_011533203.2:c.132+58_132+73del XP_011531505.1:n.132+58_132+73del
XM_017005405.2:c.132+58_132+73del XP_016860894.1:n.132+58_132+73del
NM_014748.4:c.774+58_774+73del MANE Select NP_055563.1:n.774+58_774+73del
NM_001267059.2:c.738+58_738+73del NP_001253988.1:n.738+58_738+73del
NM_001267061.2:c.714+58_714+73del NP_001253990.1:n.714+58_714+73del
NR_049782.2:n.1027+58_1027+73del
NR_049783.2:n.1000+58_1000+73del
NR_049784.2:n.976+58_976+73del
NR_049785.2:n.909+58_909+73del
NR_049786.2:n.858+58_858+73del
NR_049787.2:n.709+58_709+73del
NR_049788.2:n.639+58_639+73del
NM_001267060.2:c.699+58_699+73del NP_001253989.1:n.699+58_699+73del