Canonical Allele Identifier: CA1093716
Gene: SNX27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151693463G>A , CM000663.2:g.151693463G>A GRCh38
NC_000001.10:g.151665939G>A , CM000663.1:g.151665939G>A GRCh37
NC_000001.9:g.149932563G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368838.2:c.1116-81G>A
ENST00000368841.7:c.*1229G>A ENSP00000357834.2:n.*1229G>A
ENST00000368843.8:c.1558G>A ENSP00000357836.3:p.Glu520Lys
ENST00000458013.7:c.1558G>A MANE Select ENSP00000400333.2:p.Glu520Lys
ENST00000642349.1:c.1292G>A ENSP00000494331.1:n.1292G>A
ENST00000642376.1:c.1195G>A ENSP00000496645.1:p.Glu399Lys
ENST00000642479.1:c.*936G>A ENSP00000496775.1:n.*936G>A
ENST00000643179.1:n.1750G>A
ENST00000643937.1:n.1236G>A
ENST00000644970.1:n.1556G>A
ENST00000647328.1:n.1279G>A
ENST00000647551.1:n.5007G>A
ENST00000368838.1:c.1279G>A ENSP00000357831.1:p.Glu427Lys
ENST00000368841.6:c.*1229G>A ENSP00000357834.2:n.*1229G>A
ENST00000368843.7:c.1558G>A ENSP00000357836.3:p.Glu520Lys
ENST00000458013.6:c.1558G>A ENSP00000400333.2:p.Glu520Lys
NM_030918.5:c.1558G>A NP_112180.4:p.Glu520Lys
XM_005245509.1:c.1558G>A XP_005245566.1:p.Glu520Lys
XM_005245510.2:c.1249G>A XP_005245567.1:p.Glu417Lys
XM_005245511.3:c.1000G>A XP_005245568.1:p.Glu334Lys
XM_011510024.1:c.1255G>A XP_011508326.1:p.Glu419Lys
XM_011510025.1:c.1195G>A XP_011508327.1:p.Glu399Lys
NM_001330723.1:c.1558G>A NP_001317652.1:p.Glu520Lys
XM_005245510.3:c.1249G>A XP_005245567.1:p.Glu417Lys
XM_005245511.4:c.1000G>A XP_005245568.1:p.Glu334Lys
XM_011510024.2:c.1255G>A XP_011508326.1:p.Glu419Lys
XM_011510025.2:c.1195G>A XP_011508327.1:p.Glu399Lys
XM_017002417.1:c.1195G>A XP_016857906.1:p.Glu399Lys
XM_024450038.1:c.1000G>A XP_024305806.1:p.Glu334Lys
XM_024450039.1:c.1000G>A XP_024305807.1:p.Glu334Lys
NM_001330723.2:c.1558G>A MANE Select NP_001317652.1:p.Glu520Lys
NM_030918.6:c.1558G>A NP_112180.4:p.Glu520Lys