Canonical Allele Identifier: CA341961855

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151662202G>A , CM000663.2:g.151662202G>A	GRCh38
NC_000001.10:g.151634678G>A , CM000663.1:g.151634678G>A	GRCh37
NC_000001.9:g.149901302G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.435G>A
ENST00000368841.7:c.*509G>A	ENSP00000357834.2:n.*509G>A
ENST00000368843.8:c.838G>A	ENSP00000357836.3:p.Ala280Thr
ENST00000458013.7:c.838G>A MANE Select	ENSP00000400333.2:p.Ala280Thr
ENST00000482791.2:c.161G>A
ENST00000642349.1:c.572G>A	ENSP00000494331.1:n.572G>A
ENST00000642376.1:c.475G>A	ENSP00000496645.1:p.Ala159Thr
ENST00000642479.1:c.*216G>A	ENSP00000496775.1:n.*216G>A
ENST00000643179.1:n.646G>A
ENST00000643814.1:n.559G>A
ENST00000643937.1:n.516G>A
ENST00000644113.1:n.522G>A
ENST00000644970.1:n.836G>A
ENST00000647328.1:n.559G>A
ENST00000647454.1:n.287G>A
ENST00000368838.1:c.559G>A	ENSP00000357831.1:p.Ala187Thr
ENST00000368841.6:c.*509G>A	ENSP00000357834.2:n.*509G>A
ENST00000368843.7:c.838G>A	ENSP00000357836.3:p.Ala280Thr
ENST00000458013.6:c.838G>A	ENSP00000400333.2:p.Ala280Thr
NM_030918.5:c.838G>A	NP_112180.4:p.Ala280Thr
XM_005245509.1:c.838G>A	XP_005245566.1:p.Ala280Thr
XM_005245510.2:c.529G>A	XP_005245567.1:p.Ala177Thr
XM_005245511.3:c.280G>A	XP_005245568.1:p.Ala94Thr
XM_011510024.1:c.535G>A	XP_011508326.1:p.Ala179Thr
XM_011510025.1:c.475G>A	XP_011508327.1:p.Ala159Thr
XM_011510026.1:c.838G>A	XP_011508328.1:p.Ala280Thr
NM_001330723.1:c.838G>A	NP_001317652.1:p.Ala280Thr
XM_005245510.3:c.529G>A	XP_005245567.1:p.Ala177Thr
XM_005245511.4:c.280G>A	XP_005245568.1:p.Ala94Thr
XM_011510024.2:c.535G>A	XP_011508326.1:p.Ala179Thr
XM_011510025.2:c.475G>A	XP_011508327.1:p.Ala159Thr
XM_011510026.2:c.838G>A	XP_011508328.1:p.Ala280Thr
XM_017002417.1:c.475G>A	XP_016857906.1:p.Ala159Thr
XM_024450038.1:c.280G>A	XP_024305806.1:p.Ala94Thr
XM_024450039.1:c.280G>A	XP_024305807.1:p.Ala94Thr
NM_001330723.2:c.838G>A MANE Select	NP_001317652.1:p.Ala280Thr
NM_030918.6:c.838G>A	NP_112180.4:p.Ala280Thr