Canonical Allele Identifier: CA420752915

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151693465G>A , CM000663.2:g.151693465G>A	GRCh38
NC_000001.10:g.151665941G>A , CM000663.1:g.151665941G>A	GRCh37
NC_000001.9:g.149932565G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.1116-79G>A
ENST00000368841.7:c.*1231G>A	ENSP00000357834.2:n.*1231G>A
ENST00000368843.8:c.1560G>A	ENSP00000357836.3:p.Glu520=
ENST00000458013.7:c.1560G>A MANE Select	ENSP00000400333.2:p.Glu520=
ENST00000642349.1:c.1294G>A	ENSP00000494331.1:n.1294G>A
ENST00000642376.1:c.1197G>A	ENSP00000496645.1:p.Glu399=
ENST00000642479.1:c.*938G>A	ENSP00000496775.1:n.*938G>A
ENST00000643179.1:n.1752G>A
ENST00000643937.1:n.1238G>A
ENST00000644970.1:n.1558G>A
ENST00000647328.1:n.1281G>A
ENST00000647551.1:n.5009G>A
ENST00000368838.1:c.1281G>A	ENSP00000357831.1:p.Glu427=
ENST00000368841.6:c.*1231G>A	ENSP00000357834.2:n.*1231G>A
ENST00000368843.7:c.1560G>A	ENSP00000357836.3:p.Glu520=
ENST00000458013.6:c.1560G>A	ENSP00000400333.2:p.Glu520=
NM_030918.5:c.1560G>A	NP_112180.4:p.Glu520=
XM_005245509.1:c.1560G>A	XP_005245566.1:p.Glu520=
XM_005245510.2:c.1251G>A	XP_005245567.1:p.Glu417=
XM_005245511.3:c.1002G>A	XP_005245568.1:p.Glu334=
XM_011510024.1:c.1257G>A	XP_011508326.1:p.Glu419=
XM_011510025.1:c.1197G>A	XP_011508327.1:p.Glu399=
NM_001330723.1:c.1560G>A	NP_001317652.1:p.Glu520=
XM_005245510.3:c.1251G>A	XP_005245567.1:p.Glu417=
XM_005245511.4:c.1002G>A	XP_005245568.1:p.Glu334=
XM_011510024.2:c.1257G>A	XP_011508326.1:p.Glu419=
XM_011510025.2:c.1197G>A	XP_011508327.1:p.Glu399=
XM_017002417.1:c.1197G>A	XP_016857906.1:p.Glu399=
XM_024450038.1:c.1002G>A	XP_024305806.1:p.Glu334=
XM_024450039.1:c.1002G>A	XP_024305807.1:p.Glu334=
NM_001330723.2:c.1560G>A MANE Select	NP_001317652.1:p.Glu520=
NM_030918.6:c.1560G>A	NP_112180.4:p.Glu520=