Canonical Allele Identifier: CA2479690699
Gene: SNX27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151692534A= , CM000663.2:g.151692534A= GRCh38
NC_000001.10:g.151665010A= , CM000663.1:g.151665010A= GRCh37
NC_000001.9:g.149931634A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368838.2:c.936A=
ENST00000368841.7:c.*1010A= ENSP00000357834.2:n.*1010A=
ENST00000368843.8:c.1339A= ENSP00000357836.3:p.Ser447=
ENST00000458013.7:c.1339A= MANE Select ENSP00000400333.2:p.Ser447=
ENST00000642349.1:c.1073A= ENSP00000494331.1:n.1073A=
ENST00000642376.1:c.976A= ENSP00000496645.1:p.Ser326=
ENST00000642479.1:c.*717A= ENSP00000496775.1:n.*717A=
ENST00000643179.1:n.1147A=
ENST00000643937.1:n.1017A=
ENST00000644970.1:n.1337A=
ENST00000647328.1:n.1060A=
ENST00000647551.1:n.4788A=
ENST00000368838.1:c.1060A= ENSP00000357831.1:p.Ser354=
ENST00000368841.6:c.*1010A= ENSP00000357834.2:n.*1010A=
ENST00000368843.7:c.1339A= ENSP00000357836.3:p.Ser447=
ENST00000458013.6:c.1339A= ENSP00000400333.2:p.Ser447=
NM_030918.5:c.1339A= NP_112180.4:p.Ser447=
XM_005245509.1:c.1339A= XP_005245566.1:p.Ser447=
XM_005245510.2:c.1030A= XP_005245567.1:p.Ser344=
XM_005245511.3:c.781A= XP_005245568.1:p.Ser261=
XM_011510024.1:c.1036A= XP_011508326.1:p.Ser346=
XM_011510025.1:c.976A= XP_011508327.1:p.Ser326=
NM_001330723.1:c.1339A= NP_001317652.1:p.Ser447=
XM_005245510.3:c.1030A= XP_005245567.1:p.Ser344=
XM_005245511.4:c.781A= XP_005245568.1:p.Ser261=
XM_011510024.2:c.1036A= XP_011508326.1:p.Ser346=
XM_011510025.2:c.976A= XP_011508327.1:p.Ser326=
XM_017002417.1:c.976A= XP_016857906.1:p.Ser326=
XM_024450038.1:c.781A= XP_024305806.1:p.Ser261=
XM_024450039.1:c.781A= XP_024305807.1:p.Ser261=
NM_001330723.2:c.1339A= MANE Select NP_001317652.1:p.Ser447=
NM_030918.6:c.1339A= NP_112180.4:p.Ser447=