Canonical Allele Identifier: CA341973352
Gene: SNX27 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151612220G>T , CM000663.2:g.151612220G>T GRCh38
NC_000001.10:g.151584696G>T , CM000663.1:g.151584696G>T GRCh37
NC_000001.9:g.149851320G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368841.7:c.19G>T ENSP00000357834.2:p.Glu7Ter
ENST00000368843.8:c.19G>T ENSP00000357836.3:p.Glu7Ter
ENST00000458013.7:c.19G>T MANE Select ENSP00000400333.2:p.Glu7Ter
ENST00000642376.1:c.19G>T ENSP00000496645.1:p.Glu7Ter
ENST00000642479.1:c.19G>T ENSP00000496775.1:p.Glu7Ter
ENST00000368841.6:c.19G>T ENSP00000357834.2:p.Glu7Ter
ENST00000368843.7:c.19G>T ENSP00000357836.3:p.Glu7Ter
ENST00000458013.6:c.19G>T ENSP00000400333.2:p.Glu7Ter
NM_030918.5:c.19G>T NP_112180.4:p.Glu7Ter
XM_005245509.1:c.19G>T XP_005245566.1:p.Glu7Ter
XM_005245511.3:c.-409G>T XP_005245568.1:n.-409G>T
XM_011510024.1:c.19G>T XP_011508326.1:p.Glu7Ter
XM_011510025.1:c.19G>T XP_011508327.1:p.Glu7Ter
XM_011510026.1:c.19G>T XP_011508328.1:p.Glu7Ter
NM_001330723.1:c.19G>T NP_001317652.1:p.Glu7Ter
XM_005245511.4:c.-409G>T XP_005245568.1:n.-409G>T
XM_011510024.2:c.19G>T XP_011508326.1:p.Glu7Ter
XM_011510025.2:c.19G>T XP_011508327.1:p.Glu7Ter
XM_011510026.2:c.19G>T XP_011508328.1:p.Glu7Ter
XM_017002417.1:c.19G>T XP_016857906.1:p.Glu7Ter
XM_024450038.1:c.-308G>T XP_024305806.1:n.-308G>T
NM_001330723.2:c.19G>T MANE Select NP_001317652.1:p.Glu7Ter
NM_030918.6:c.19G>T NP_112180.4:p.Glu7Ter