Canonical Allele Identifier: CA420750865

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151668491T>C , CM000663.2:g.151668491T>C	GRCh38
NC_000001.10:g.151640967T>C , CM000663.1:g.151640967T>C	GRCh37
NC_000001.9:g.149907591T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.602T>C
ENST00000368841.7:c.*676T>C	ENSP00000357834.2:n.*676T>C
ENST00000368843.8:c.1005T>C	ENSP00000357836.3:p.Asn335=
ENST00000458013.7:c.1005T>C MANE Select	ENSP00000400333.2:p.Asn335=
ENST00000482791.2:c.328T>C
ENST00000642349.1:c.739T>C	ENSP00000494331.1:n.739T>C
ENST00000642376.1:c.642T>C	ENSP00000496645.1:p.Asn214=
ENST00000642479.1:c.*383T>C	ENSP00000496775.1:n.*383T>C
ENST00000643179.1:n.813T>C
ENST00000643937.1:n.683T>C
ENST00000644113.1:n.689T>C
ENST00000644970.1:n.1003T>C
ENST00000647328.1:n.726T>C
ENST00000368838.1:c.726T>C	ENSP00000357831.1:p.Asn242=
ENST00000368841.6:c.*676T>C	ENSP00000357834.2:n.*676T>C
ENST00000368843.7:c.1005T>C	ENSP00000357836.3:p.Asn335=
ENST00000458013.6:c.1005T>C	ENSP00000400333.2:p.Asn335=
ENST00000482791.1:n.126T>C
NM_030918.5:c.1005T>C	NP_112180.4:p.Asn335=
XM_005245509.1:c.1005T>C	XP_005245566.1:p.Asn335=
XM_005245510.2:c.696T>C	XP_005245567.1:p.Asn232=
XM_005245511.3:c.447T>C	XP_005245568.1:p.Asn149=
XM_011510024.1:c.702T>C	XP_011508326.1:p.Asn234=
XM_011510025.1:c.642T>C	XP_011508327.1:p.Asn214=
XM_011510026.1:c.1005T>C	XP_011508328.1:p.Asn335=
NM_001330723.1:c.1005T>C	NP_001317652.1:p.Asn335=
XM_005245510.3:c.696T>C	XP_005245567.1:p.Asn232=
XM_005245511.4:c.447T>C	XP_005245568.1:p.Asn149=
XM_011510024.2:c.702T>C	XP_011508326.1:p.Asn234=
XM_011510025.2:c.642T>C	XP_011508327.1:p.Asn214=
XM_011510026.2:c.1005T>C	XP_011508328.1:p.Asn335=
XM_017002417.1:c.642T>C	XP_016857906.1:p.Asn214=
XM_024450038.1:c.447T>C	XP_024305806.1:p.Asn149=
XM_024450039.1:c.447T>C	XP_024305807.1:p.Asn149=
NM_001330723.2:c.1005T>C MANE Select	NP_001317652.1:p.Asn335=
NM_030918.6:c.1005T>C	NP_112180.4:p.Asn335=