Canonical Allele Identifier: CA420751840

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151683415G>A , CM000663.2:g.151683415G>A	GRCh38
NC_000001.10:g.151655891G>A , CM000663.1:g.151655891G>A	GRCh37
NC_000001.9:g.149922515G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.806G>A
ENST00000368841.7:c.*880G>A	ENSP00000357834.2:n.*880G>A
ENST00000368843.8:c.1209G>A	ENSP00000357836.3:p.Gln403=
ENST00000458013.7:c.1209G>A MANE Select	ENSP00000400333.2:p.Gln403=
ENST00000642349.1:c.943G>A	ENSP00000494331.1:n.943G>A
ENST00000642376.1:c.846G>A	ENSP00000496645.1:p.Gln282=
ENST00000642479.1:c.*587G>A	ENSP00000496775.1:n.*587G>A
ENST00000643179.1:n.1017G>A
ENST00000643937.1:n.887G>A
ENST00000644113.1:n.893G>A
ENST00000644970.1:n.1207G>A
ENST00000647328.1:n.930G>A
ENST00000647551.1:n.4658G>A
ENST00000368838.1:c.930G>A	ENSP00000357831.1:p.Gln310=
ENST00000368841.6:c.*880G>A	ENSP00000357834.2:n.*880G>A
ENST00000368843.7:c.1209G>A	ENSP00000357836.3:p.Gln403=
ENST00000458013.6:c.1209G>A	ENSP00000400333.2:p.Gln403=
NM_030918.5:c.1209G>A	NP_112180.4:p.Gln403=
XM_005245509.1:c.1209G>A	XP_005245566.1:p.Gln403=
XM_005245510.2:c.900G>A	XP_005245567.1:p.Gln300=
XM_005245511.3:c.651G>A	XP_005245568.1:p.Gln217=
XM_011510024.1:c.906G>A	XP_011508326.1:p.Gln302=
XM_011510025.1:c.846G>A	XP_011508327.1:p.Gln282=
NM_001330723.1:c.1209G>A	NP_001317652.1:p.Gln403=
XM_005245510.3:c.900G>A	XP_005245567.1:p.Gln300=
XM_005245511.4:c.651G>A	XP_005245568.1:p.Gln217=
XM_011510024.2:c.906G>A	XP_011508326.1:p.Gln302=
XM_011510025.2:c.846G>A	XP_011508327.1:p.Gln282=
XM_017002417.1:c.846G>A	XP_016857906.1:p.Gln282=
XM_024450038.1:c.651G>A	XP_024305806.1:p.Gln217=
XM_024450039.1:c.651G>A	XP_024305807.1:p.Gln217=
NM_001330723.2:c.1209G>A MANE Select	NP_001317652.1:p.Gln403=
NM_030918.6:c.1209G>A	NP_112180.4:p.Gln403=