Canonical Allele Identifier: CA767386508
Gene: SNX17 HGNC NCBI

Linked Data

dbSNP Id: rs1311121554

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27375164_27375176del , CM000664.2:g.27375164_27375176del GRCh38
NC_000002.11:g.27598031_27598043del , CM000664.1:g.27598031_27598043del GRCh37
NC_000002.10:g.27451535_27451547del NCBI36
NG_009305.1:g.282_294del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233575.7:c.774+11_774+23del MANE Select ENSP00000233575.2:n.774+11_774+23del
ENST00000233575.6:c.774+11_774+23del ENSP00000233575.2:n.774+11_774+23del
ENST00000427123.5:c.*584+11_*584+23del ENSP00000405399.1:n.*584+11_*584+23del
ENST00000440760.5:c.*619+11_*619+23del ENSP00000399727.1:n.*619+11_*619+23del
ENST00000453453.1:c.*301+11_*301+23del ENSP00000401922.1:n.*301+11_*301+23del
ENST00000493711.1:n.491+11_491+23del
ENST00000494893.5:n.950+11_950+23del
ENST00000537606.5:c.699+11_699+23del ENSP00000439208.1:n.699+11_699+23del
NM_001267059.1:c.738+11_738+23del NP_001253988.1:n.738+11_738+23del
NM_001267060.1:c.699+11_699+23del NP_001253989.1:n.699+11_699+23del
NM_001267061.1:c.714+11_714+23del NP_001253990.1:n.714+11_714+23del
NM_014748.3:c.774+11_774+23del NP_055563.1:n.774+11_774+23del
NR_049782.1:n.1147+11_1147+23del
NR_049783.1:n.1120+11_1120+23del
NR_049784.1:n.1096+11_1096+23del
NR_049785.1:n.1029+11_1029+23del
NR_049786.1:n.978+11_978+23del
NR_049787.1:n.829+11_829+23del
NR_049788.1:n.759+11_759+23del
XM_011533203.1:c.132+11_132+23del XP_011531505.1:n.132+11_132+23del
XM_011533203.2:c.132+11_132+23del XP_011531505.1:n.132+11_132+23del
XM_017005405.2:c.132+11_132+23del XP_016860894.1:n.132+11_132+23del
NM_014748.4:c.774+11_774+23del MANE Select NP_055563.1:n.774+11_774+23del
NM_001267059.2:c.738+11_738+23del NP_001253988.1:n.738+11_738+23del
NM_001267061.2:c.714+11_714+23del NP_001253990.1:n.714+11_714+23del
NR_049782.2:n.1027+11_1027+23del
NR_049783.2:n.1000+11_1000+23del
NR_049784.2:n.976+11_976+23del
NR_049785.2:n.909+11_909+23del
NR_049786.2:n.858+11_858+23del
NR_049787.2:n.709+11_709+23del
NR_049788.2:n.639+11_639+23del
NM_001267060.2:c.699+11_699+23del NP_001253989.1:n.699+11_699+23del