Canonical Allele Identifier: CA1873106791
Gene: SNX30 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112788132A= , CM000671.2:g.112788132A= GRCh38
NC_000009.11:g.115550412A= , CM000671.1:g.115550412A= GRCh37
NC_000009.10:g.114590233A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374232.8:c.157-16644A= MANE Select ENSP00000363349.3:n.157-16644A=
ENST00000374232.7:c.157-16644A= ENSP00000363349.3:n.157-16644A=
NM_001012994.1:c.157-16644A= NP_001013012.1:n.157-16644A=
XM_005251986.3:c.-156-16644A= XP_005252043.1:n.-156-16644A=
XM_011518691.1:c.157-16644A= XP_011516993.1:n.157-16644A=
XM_011518691.2:c.157-16644A= XP_011516993.1:n.157-16644A=
XM_017014716.2:c.34-16644A= XP_016870205.1:n.34-16644A=
XM_024447544.1:c.-156-16644A= XP_024303312.1:n.-156-16644A=
NM_001012994.2:c.157-16644A= MANE Select NP_001013012.1:n.157-16644A=
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