Canonical Allele Identifier: CA2658341354
Gene: SNX17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27375048_27375049insCC , CM000664.2:g.27375048_27375049insCC GRCh38
NC_000002.11:g.27597915_27597916insCC , CM000664.1:g.27597915_27597916insCC GRCh37
NC_000002.10:g.27451419_27451420insCC NCBI36
NG_009305.1:g.409_410insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233575.7:c.682-13_682-12insCC MANE Select ENSP00000233575.2:n.682-13_682-12insCC
ENST00000233575.6:c.682-13_682-12insCC ENSP00000233575.2:n.682-13_682-12insCC
ENST00000427123.5:c.*492-13_*492-12insCC ENSP00000405399.1:n.*492-13_*492-12insCC
ENST00000440760.5:c.*527-13_*527-12insCC ENSP00000399727.1:n.*527-13_*527-12insCC
ENST00000453453.1:c.*209-13_*209-12insCC ENSP00000401922.1:n.*209-13_*209-12insCC
ENST00000493711.1:n.386_387insCC
ENST00000494893.5:n.858-13_858-12insCC
ENST00000537606.5:c.607-13_607-12insCC ENSP00000439208.1:n.607-13_607-12insCC
NM_001267059.1:c.646-13_646-12insCC NP_001253988.1:n.646-13_646-12insCC
NM_001267060.1:c.607-13_607-12insCC NP_001253989.1:n.607-13_607-12insCC
NM_001267061.1:c.622-13_622-12insCC NP_001253990.1:n.622-13_622-12insCC
NM_014748.3:c.682-13_682-12insCC NP_055563.1:n.682-13_682-12insCC
NR_049782.1:n.1055-13_1055-12insCC
NR_049783.1:n.1028-13_1028-12insCC
NR_049784.1:n.1004-13_1004-12insCC
NR_049785.1:n.937-13_937-12insCC
NR_049786.1:n.886-13_886-12insCC
NR_049787.1:n.737-13_737-12insCC
NR_049788.1:n.667-13_667-12insCC
XM_011533203.1:c.40-13_40-12insCC XP_011531505.1:n.40-13_40-12insCC
XM_011533203.2:c.40-13_40-12insCC XP_011531505.1:n.40-13_40-12insCC
XM_017005405.2:c.40-13_40-12insCC XP_016860894.1:n.40-13_40-12insCC
NM_014748.4:c.682-13_682-12insCC MANE Select NP_055563.1:n.682-13_682-12insCC
NM_001267059.2:c.646-13_646-12insCC NP_001253988.1:n.646-13_646-12insCC
NM_001267061.2:c.622-13_622-12insCC NP_001253990.1:n.622-13_622-12insCC
NR_049782.2:n.935-13_935-12insCC
NR_049783.2:n.908-13_908-12insCC
NR_049784.2:n.884-13_884-12insCC
NR_049785.2:n.817-13_817-12insCC
NR_049786.2:n.766-13_766-12insCC
NR_049787.2:n.617-13_617-12insCC
NR_049788.2:n.547-13_547-12insCC
NM_001267060.2:c.607-13_607-12insCC NP_001253989.1:n.607-13_607-12insCC