Canonical Allele Identifier: CA420752460

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692964A>G , CM000663.2:g.151692964A>G	GRCh38
NC_000001.10:g.151665440A>G , CM000663.1:g.151665440A>G	GRCh37
NC_000001.9:g.149932064A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.1040A>G
ENST00000368841.7:c.*1114A>G	ENSP00000357834.2:n.*1114A>G
ENST00000368843.8:c.1443A>G	ENSP00000357836.3:p.Glu481=
ENST00000458013.7:c.1443A>G MANE Select	ENSP00000400333.2:p.Glu481=
ENST00000642349.1:c.1177A>G	ENSP00000494331.1:n.1177A>G
ENST00000642376.1:c.1080A>G	ENSP00000496645.1:p.Glu360=
ENST00000642479.1:c.*821A>G	ENSP00000496775.1:n.*821A>G
ENST00000643179.1:n.1251A>G
ENST00000643937.1:n.1121A>G
ENST00000644970.1:n.1441A>G
ENST00000647328.1:n.1164A>G
ENST00000647551.1:n.4892A>G
ENST00000368838.1:c.1164A>G	ENSP00000357831.1:p.Glu388=
ENST00000368841.6:c.*1114A>G	ENSP00000357834.2:n.*1114A>G
ENST00000368843.7:c.1443A>G	ENSP00000357836.3:p.Glu481=
ENST00000458013.6:c.1443A>G	ENSP00000400333.2:p.Glu481=
NM_030918.5:c.1443A>G	NP_112180.4:p.Glu481=
XM_005245509.1:c.1443A>G	XP_005245566.1:p.Glu481=
XM_005245510.2:c.1134A>G	XP_005245567.1:p.Glu378=
XM_005245511.3:c.885A>G	XP_005245568.1:p.Glu295=
XM_011510024.1:c.1140A>G	XP_011508326.1:p.Glu380=
XM_011510025.1:c.1080A>G	XP_011508327.1:p.Glu360=
NM_001330723.1:c.1443A>G	NP_001317652.1:p.Glu481=
XM_005245510.3:c.1134A>G	XP_005245567.1:p.Glu378=
XM_005245511.4:c.885A>G	XP_005245568.1:p.Glu295=
XM_011510024.2:c.1140A>G	XP_011508326.1:p.Glu380=
XM_011510025.2:c.1080A>G	XP_011508327.1:p.Glu360=
XM_017002417.1:c.1080A>G	XP_016857906.1:p.Glu360=
XM_024450038.1:c.885A>G	XP_024305806.1:p.Glu295=
XM_024450039.1:c.885A>G	XP_024305807.1:p.Glu295=
NM_001330723.2:c.1443A>G MANE Select	NP_001317652.1:p.Glu481=
NM_030918.6:c.1443A>G	NP_112180.4:p.Glu481=