Canonical Allele Identifier: CA341966569

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151668621T>C , CM000663.2:g.151668621T>C	GRCh38
NC_000001.10:g.151641097T>C , CM000663.1:g.151641097T>C	GRCh37
NC_000001.9:g.149907721T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.732T>C
ENST00000368841.7:c.*806T>C	ENSP00000357834.2:n.*806T>C
ENST00000368843.8:c.1135T>C	ENSP00000357836.3:p.Tyr379His
ENST00000458013.7:c.1135T>C MANE Select	ENSP00000400333.2:p.Tyr379His
ENST00000482791.2:c.458T>C
ENST00000642349.1:c.869T>C	ENSP00000494331.1:n.869T>C
ENST00000642376.1:c.772T>C	ENSP00000496645.1:p.Tyr258His
ENST00000642479.1:c.*513T>C	ENSP00000496775.1:n.*513T>C
ENST00000643179.1:n.943T>C
ENST00000643937.1:n.813T>C
ENST00000644113.1:n.819T>C
ENST00000644970.1:n.1133T>C
ENST00000647328.1:n.856T>C
ENST00000368838.1:c.856T>C	ENSP00000357831.1:p.Tyr286His
ENST00000368841.6:c.*806T>C	ENSP00000357834.2:n.*806T>C
ENST00000368843.7:c.1135T>C	ENSP00000357836.3:p.Tyr379His
ENST00000458013.6:c.1135T>C	ENSP00000400333.2:p.Tyr379His
ENST00000482791.1:n.256T>C
NM_030918.5:c.1135T>C	NP_112180.4:p.Tyr379His
XM_005245509.1:c.1135T>C	XP_005245566.1:p.Tyr379His
XM_005245510.2:c.826T>C	XP_005245567.1:p.Tyr276His
XM_005245511.3:c.577T>C	XP_005245568.1:p.Tyr193His
XM_011510024.1:c.832T>C	XP_011508326.1:p.Tyr278His
XM_011510025.1:c.772T>C	XP_011508327.1:p.Tyr258His
XM_011510026.1:c.1135T>C	XP_011508328.1:p.Tyr379His
NM_001330723.1:c.1135T>C	NP_001317652.1:p.Tyr379His
XM_005245510.3:c.826T>C	XP_005245567.1:p.Tyr276His
XM_005245511.4:c.577T>C	XP_005245568.1:p.Tyr193His
XM_011510024.2:c.832T>C	XP_011508326.1:p.Tyr278His
XM_011510025.2:c.772T>C	XP_011508327.1:p.Tyr258His
XM_011510026.2:c.1135T>C	XP_011508328.1:p.Tyr379His
XM_017002417.1:c.772T>C	XP_016857906.1:p.Tyr258His
XM_024450038.1:c.577T>C	XP_024305806.1:p.Tyr193His
XM_024450039.1:c.577T>C	XP_024305807.1:p.Tyr193His
NM_001330723.2:c.1135T>C MANE Select	NP_001317652.1:p.Tyr379His
NM_030918.6:c.1135T>C	NP_112180.4:p.Tyr379His