Canonical Allele Identifier: CA341963830

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151665934C>G , CM000663.2:g.151665934C>G	GRCh38
NC_000001.10:g.151638410C>G , CM000663.1:g.151638410C>G	GRCh37
NC_000001.9:g.149905034C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.505C>G
ENST00000368841.7:c.*579C>G	ENSP00000357834.2:n.*579C>G
ENST00000368843.8:c.908C>G	ENSP00000357836.3:p.Ala303Gly
ENST00000458013.7:c.908C>G MANE Select	ENSP00000400333.2:p.Ala303Gly
ENST00000482791.2:c.231C>G
ENST00000642349.1:c.642C>G	ENSP00000494331.1:n.642C>G
ENST00000642376.1:c.545C>G	ENSP00000496645.1:p.Ala182Gly
ENST00000642479.1:c.*286C>G	ENSP00000496775.1:n.*286C>G
ENST00000643179.1:n.716C>G
ENST00000643814.1:n.629C>G
ENST00000643937.1:n.586C>G
ENST00000644113.1:n.592C>G
ENST00000644970.1:n.906C>G
ENST00000647328.1:n.629C>G
ENST00000368838.1:c.629C>G	ENSP00000357831.1:p.Ala210Gly
ENST00000368841.6:c.*579C>G	ENSP00000357834.2:n.*579C>G
ENST00000368843.7:c.908C>G	ENSP00000357836.3:p.Ala303Gly
ENST00000458013.6:c.908C>G	ENSP00000400333.2:p.Ala303Gly
ENST00000482791.1:n.29C>G
NM_030918.5:c.908C>G	NP_112180.4:p.Ala303Gly
XM_005245509.1:c.908C>G	XP_005245566.1:p.Ala303Gly
XM_005245510.2:c.599C>G	XP_005245567.1:p.Ala200Gly
XM_005245511.3:c.350C>G	XP_005245568.1:p.Ala117Gly
XM_011510024.1:c.605C>G	XP_011508326.1:p.Ala202Gly
XM_011510025.1:c.545C>G	XP_011508327.1:p.Ala182Gly
XM_011510026.1:c.908C>G	XP_011508328.1:p.Ala303Gly
NM_001330723.1:c.908C>G	NP_001317652.1:p.Ala303Gly
XM_005245510.3:c.599C>G	XP_005245567.1:p.Ala200Gly
XM_005245511.4:c.350C>G	XP_005245568.1:p.Ala117Gly
XM_011510024.2:c.605C>G	XP_011508326.1:p.Ala202Gly
XM_011510025.2:c.545C>G	XP_011508327.1:p.Ala182Gly
XM_011510026.2:c.908C>G	XP_011508328.1:p.Ala303Gly
XM_017002417.1:c.545C>G	XP_016857906.1:p.Ala182Gly
XM_024450038.1:c.350C>G	XP_024305806.1:p.Ala117Gly
XM_024450039.1:c.350C>G	XP_024305807.1:p.Ala117Gly
NM_001330723.2:c.908C>G MANE Select	NP_001317652.1:p.Ala303Gly
NM_030918.6:c.908C>G	NP_112180.4:p.Ala303Gly