Canonical Allele Identifier: CA2658341923
Gene: SNX17 HGNC NCBI

Linked Data

dbSNP Id: rs2148404281

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27375556_27375557insAGTGCCTACTTGCGCTTTGAT , CM000664.2:g.27375556_27375557insAGTGCCTACTTGCGCTTTGAT GRCh38
NC_000002.11:g.27598423_27598424insAGTGCCTACTTGCGCTTTGAT , CM000664.1:g.27598423_27598424insAGTGCCTACTTGCGCTTTGAT GRCh37
NC_000002.10:g.27451927_27451928insAGTGCCTACTTGCGCTTTGAT NCBI36
NG_028219.1:g.10204_10205insGCACTATCAAAGCGCAAGTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233575.7:c.825_826insAGTGCCTACTTGCGCTTTGAT MANE Select ENSP00000233575.2:p.Asp275_Ala276insSerAlaTyrLeuArgPheAsp
ENST00000233575.6:c.825_826insAGTGCCTACTTGCGCTTTGAT ENSP00000233575.2:p.Asp275_Ala276insSerAlaTyrLeuArgPheAsp
ENST00000427123.5:c.*635_*636insAGTGCCTACTTGCGCTTTGAT ENSP00000405399.1:n.*635_*636insAGTGCCTACTTGCGCTTTGAT
ENST00000440760.5:c.*670_*671insAGTGCCTACTTGCGCTTTGAT ENSP00000399727.1:n.*670_*671insAGTGCCTACTTGCGCTTTGAT
ENST00000453453.1:c.*352_*353insAGTGCCTACTTGCGCTTTGAT ENSP00000401922.1:n.*352_*353insAGTGCCTACTTGCGCTTTGAT
ENST00000493711.1:n.542_543insAGTGCCTACTTGCGCTTTGAT
ENST00000537606.5:c.750_751insAGTGCCTACTTGCGCTTTGAT ENSP00000439208.1:p.Asp250_Ala251insSerAlaTyrLeuArgPheAsp
NM_001267059.1:c.789_790insAGTGCCTACTTGCGCTTTGAT NP_001253988.1:p.Asp263_Ala264insSerAlaTyrLeuArgPheAsp
NM_001267060.1:c.750_751insAGTGCCTACTTGCGCTTTGAT NP_001253989.1:p.Asp250_Ala251insSerAlaTyrLeuArgPheAsp
NM_001267061.1:c.765_766insAGTGCCTACTTGCGCTTTGAT NP_001253990.1:p.Asp255_Ala256insSerAlaTyrLeuArgPheAsp
NM_014748.3:c.825_826insAGTGCCTACTTGCGCTTTGAT NP_055563.1:p.Asp275_Ala276insSerAlaTyrLeuArgPheAsp
NR_049782.1:n.1198_1199insAGTGCCTACTTGCGCTTTGAT
NR_049783.1:n.1171_1172insAGTGCCTACTTGCGCTTTGAT
NR_049784.1:n.1147_1148insAGTGCCTACTTGCGCTTTGAT
NR_049785.1:n.1080_1081insAGTGCCTACTTGCGCTTTGAT
NR_049786.1:n.1029_1030insAGTGCCTACTTGCGCTTTGAT
NR_049787.1:n.880_881insAGTGCCTACTTGCGCTTTGAT
NR_049788.1:n.810_811insAGTGCCTACTTGCGCTTTGAT
XM_011533203.1:c.183_184insAGTGCCTACTTGCGCTTTGAT XP_011531505.1:p.Asp61_Ala62insSerAlaTyrLeuArgPheAsp
XM_011533203.2:c.183_184insAGTGCCTACTTGCGCTTTGAT XP_011531505.1:p.Asp61_Ala62insSerAlaTyrLeuArgPheAsp
XM_017005405.2:c.183_184insAGTGCCTACTTGCGCTTTGAT XP_016860894.1:p.Asp61_Ala62insSerAlaTyrLeuArgPheAsp
NM_014748.4:c.825_826insAGTGCCTACTTGCGCTTTGAT MANE Select NP_055563.1:p.Asp275_Ala276insSerAlaTyrLeuArgPheAsp
NM_001267059.2:c.789_790insAGTGCCTACTTGCGCTTTGAT NP_001253988.1:p.Asp263_Ala264insSerAlaTyrLeuArgPheAsp
NM_001267061.2:c.765_766insAGTGCCTACTTGCGCTTTGAT NP_001253990.1:p.Asp255_Ala256insSerAlaTyrLeuArgPheAsp
NR_049782.2:n.1078_1079insAGTGCCTACTTGCGCTTTGAT
NR_049783.2:n.1051_1052insAGTGCCTACTTGCGCTTTGAT
NR_049784.2:n.1027_1028insAGTGCCTACTTGCGCTTTGAT
NR_049785.2:n.960_961insAGTGCCTACTTGCGCTTTGAT
NR_049786.2:n.909_910insAGTGCCTACTTGCGCTTTGAT
NR_049787.2:n.760_761insAGTGCCTACTTGCGCTTTGAT
NR_049788.2:n.690_691insAGTGCCTACTTGCGCTTTGAT
NM_001267060.2:c.750_751insAGTGCCTACTTGCGCTTTGAT NP_001253989.1:p.Asp250_Ala251insSerAlaTyrLeuArgPheAsp