Canonical Allele Identifier: CA2479678738

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151662208_151662210dup , CM000663.2:g.151662208_151662210dup	GRCh38
NC_000001.10:g.151634684_151634686dup , CM000663.1:g.151634684_151634686dup	GRCh37
NC_000001.9:g.149901308_149901310dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.441_443dup
ENST00000368841.7:c.*515_*517dup	ENSP00000357834.2:n.*515_*517dup
ENST00000368843.8:c.844_846dup	ENSP00000357836.3:p.Pro282_Asp283insPro
ENST00000458013.7:c.844_846dup MANE Select	ENSP00000400333.2:p.Pro282_Asp283insPro
ENST00000482791.2:c.167_169dup
ENST00000642349.1:c.578_580dup	ENSP00000494331.1:n.578_580dup
ENST00000642376.1:c.481_483dup	ENSP00000496645.1:p.Pro161_Asp162insPro
ENST00000642479.1:c.*222_*224dup	ENSP00000496775.1:n.*222_*224dup
ENST00000643179.1:n.652_654dup
ENST00000643814.1:n.565_567dup
ENST00000643937.1:n.522_524dup
ENST00000644113.1:n.528_530dup
ENST00000644970.1:n.842_844dup
ENST00000647328.1:n.565_567dup
ENST00000647454.1:n.293_295dup
ENST00000368838.1:c.565_567dup	ENSP00000357831.1:p.Pro189_Asp190insPro
ENST00000368841.6:c.*515_*517dup	ENSP00000357834.2:n.*515_*517dup
ENST00000368843.7:c.844_846dup	ENSP00000357836.3:p.Pro282_Asp283insPro
ENST00000458013.6:c.844_846dup	ENSP00000400333.2:p.Pro282_Asp283insPro
NM_030918.5:c.844_846dup	NP_112180.4:p.Pro282_Asp283insPro
XM_005245509.1:c.844_846dup	XP_005245566.1:p.Pro282_Asp283insPro
XM_005245510.2:c.535_537dup	XP_005245567.1:p.Pro179_Asp180insPro
XM_005245511.3:c.286_288dup	XP_005245568.1:p.Pro96_Asp97insPro
XM_011510024.1:c.541_543dup	XP_011508326.1:p.Pro181_Asp182insPro
XM_011510025.1:c.481_483dup	XP_011508327.1:p.Pro161_Asp162insPro
XM_011510026.1:c.844_846dup	XP_011508328.1:p.Pro282_Asp283insPro
NM_001330723.1:c.844_846dup	NP_001317652.1:p.Pro282_Asp283insPro
XM_005245510.3:c.535_537dup	XP_005245567.1:p.Pro179_Asp180insPro
XM_005245511.4:c.286_288dup	XP_005245568.1:p.Pro96_Asp97insPro
XM_011510024.2:c.541_543dup	XP_011508326.1:p.Pro181_Asp182insPro
XM_011510025.2:c.481_483dup	XP_011508327.1:p.Pro161_Asp162insPro
XM_011510026.2:c.844_846dup	XP_011508328.1:p.Pro282_Asp283insPro
XM_017002417.1:c.481_483dup	XP_016857906.1:p.Pro161_Asp162insPro
XM_024450038.1:c.286_288dup	XP_024305806.1:p.Pro96_Asp97insPro
XM_024450039.1:c.286_288dup	XP_024305807.1:p.Pro96_Asp97insPro
NM_001330723.2:c.844_846dup MANE Select	NP_001317652.1:p.Pro282_Asp283insPro
NM_030918.6:c.844_846dup	NP_112180.4:p.Pro282_Asp283insPro