Canonical Allele Identifier: CA341972939

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692947C>T , CM000663.2:g.151692947C>T	GRCh38
NC_000001.10:g.151665423C>T , CM000663.1:g.151665423C>T	GRCh37
NC_000001.9:g.149932047C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001330723.2:c.1426C>T MANE Select	NP_001317652.1:p.Arg476Ter
ENST00000458013.7:c.1426C>T MANE Select	ENSP00000400333.2:p.Arg476Ter
NM_001330723.1:c.1426C>T	NP_001317652.1:p.Arg476Ter
NM_030918.5:c.1426C>T	NP_112180.4:p.Arg476Ter
NM_030918.6:c.1426C>T	NP_112180.4:p.Arg476Ter
ENST00000368838.1:c.1147C>T	ENSP00000357831.1:p.Arg383Ter
ENST00000368838.2:c.1023C>T
ENST00000368841.6:c.*1097C>T	ENSP00000357834.2:n.*1097C>T
ENST00000368841.7:c.*1097C>T	ENSP00000357834.2:n.*1097C>T
ENST00000368843.7:c.1426C>T	ENSP00000357836.3:p.Arg476Ter
ENST00000368843.8:c.1426C>T	ENSP00000357836.3:p.Arg476Ter
ENST00000458013.6:c.1426C>T	ENSP00000400333.2:p.Arg476Ter
ENST00000642349.1:c.1160C>T	ENSP00000494331.1:n.1160C>T
ENST00000642376.1:c.1063C>T	ENSP00000496645.1:p.Arg355Ter
ENST00000642479.1:c.*804C>T	ENSP00000496775.1:n.*804C>T
ENST00000643179.1:n.1234C>T
ENST00000643937.1:n.1104C>T
ENST00000644970.1:n.1424C>T
ENST00000647328.1:n.1147C>T
ENST00000647551.1:n.4875C>T
XM_005245509.1:c.1426C>T	XP_005245566.1:p.Arg476Ter
XM_005245510.2:c.1117C>T	XP_005245567.1:p.Arg373Ter
XM_005245510.3:c.1117C>T	XP_005245567.1:p.Arg373Ter
XM_005245511.3:c.868C>T	XP_005245568.1:p.Arg290Ter
XM_005245511.4:c.868C>T	XP_005245568.1:p.Arg290Ter
XM_011510024.1:c.1123C>T	XP_011508326.1:p.Arg375Ter
XM_011510024.2:c.1123C>T	XP_011508326.1:p.Arg375Ter
XM_011510025.1:c.1063C>T	XP_011508327.1:p.Arg355Ter
XM_011510025.2:c.1063C>T	XP_011508327.1:p.Arg355Ter
XM_017002417.1:c.1063C>T	XP_016857906.1:p.Arg355Ter
XM_024450038.1:c.868C>T	XP_024305806.1:p.Arg290Ter
XM_024450039.1:c.868C>T	XP_024305807.1:p.Arg290Ter