Canonical Allele Identifier: CA278462863
Gene: SNX29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.12547258C>T , CM000678.2:g.12547258C>T GRCh38
NC_000016.9:g.12641115C>T , CM000678.1:g.12641115C>T GRCh37
NC_000016.8:g.12548616C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000566228.6:c.2319-21248C>T MANE Select ENSP00000456480.1:n.2319-21248C>T
ENST00000566228.5:c.2319-21248C>T ENSP00000456480.1:n.2319-21248C>T
NM_032167.4:c.2319-21248C>T NP_115543.3:n.2319-21248C>T
XM_005255682.2:c.2349-21248C>T XP_005255739.1:n.2349-21248C>T
XM_011522738.1:c.2460-13663C>T XP_011521040.1:n.2460-13663C>T
XM_011522741.1:c.2460-21248C>T XP_011521043.1:n.2460-21248C>T
XR_933082.1:n.2021G>A
XM_005255682.4:c.2349-21248C>T XP_005255739.1:n.2349-21248C>T
XM_011522738.3:c.2460-13663C>T XP_011521040.1:n.2460-13663C>T
XM_011522741.3:c.2460-21248C>T XP_011521043.1:n.2460-21248C>T
XM_017023871.2:c.2433-13663C>T XP_016879360.1:n.2433-13663C>T
XM_017023872.1:c.2430-13663C>T XP_016879361.1:n.2430-13663C>T
XM_017023873.2:c.2349-13663C>T XP_016879362.1:n.2349-13663C>T
XM_017023874.1:c.2319-13663C>T XP_016879363.1:n.2319-13663C>T
XM_017023878.2:c.1050-13663C>T XP_016879367.1:n.1050-13663C>T
XM_024450491.1:c.1974-13663C>T XP_024306259.1:n.1974-13663C>T
XR_001752024.2:n.2679-13663C>T
XR_002957889.1:n.5929G>A
XR_002957890.1:n.6168G>A
XR_002957891.1:n.5816G>A
XR_002957892.1:n.5929G>A
XR_002957893.1:n.5929G>A
XR_933080.3:n.5814G>A
NM_032167.5:c.2319-21248C>T MANE Select NP_115543.3:n.2319-21248C>T
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