Canonical Allele Identifier: CA889363787

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151668653_151668655del , CM000663.2:g.151668653_151668655del	GRCh38
NC_000001.10:g.151641129_151641131del , CM000663.1:g.151641129_151641131del	GRCh37
NC_000001.9:g.149907753_149907755del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.746+18_746+20del
ENST00000368841.7:c.*820+18_*820+20del	ENSP00000357834.2:n.*820+18_*820+20del
ENST00000368843.8:c.1149+18_1149+20del	ENSP00000357836.3:n.1149+18_1149+20del
ENST00000458013.7:c.1149+18_1149+20del MANE Select	ENSP00000400333.2:n.1149+18_1149+20del
ENST00000482791.2:c.472+18_472+20del
ENST00000642349.1:c.883+18_883+20del	ENSP00000494331.1:n.883+18_883+20del
ENST00000642376.1:c.786+18_786+20del	ENSP00000496645.1:n.786+18_786+20del
ENST00000642479.1:c.*527+18_*527+20del	ENSP00000496775.1:n.*527+18_*527+20del
ENST00000643179.1:n.957+18_957+20del
ENST00000643937.1:n.827+18_827+20del
ENST00000644113.1:n.833+18_833+20del
ENST00000644970.1:n.1147+18_1147+20del
ENST00000647328.1:n.870+18_870+20del
ENST00000368838.1:c.870+18_870+20del	ENSP00000357831.1:n.870+18_870+20del
ENST00000368841.6:c.*820+18_*820+20del	ENSP00000357834.2:n.*820+18_*820+20del
ENST00000368843.7:c.1149+18_1149+20del	ENSP00000357836.3:n.1149+18_1149+20del
ENST00000458013.6:c.1149+18_1149+20del	ENSP00000400333.2:n.1149+18_1149+20del
ENST00000482791.1:n.270+18_270+20del
NM_030918.5:c.1149+18_1149+20del	NP_112180.4:n.1149+18_1149+20del
XM_005245509.1:c.1149+18_1149+20del	XP_005245566.1:n.1149+18_1149+20del
XM_005245510.2:c.840+18_840+20del	XP_005245567.1:n.840+18_840+20del
XM_005245511.3:c.591+18_591+20del	XP_005245568.1:n.591+18_591+20del
XM_011510024.1:c.846+18_846+20del	XP_011508326.1:n.846+18_846+20del
XM_011510025.1:c.786+18_786+20del	XP_011508327.1:n.786+18_786+20del
XM_011510026.1:c.1149+18_1149+20del	XP_011508328.1:n.1149+18_1149+20del
NM_001330723.1:c.1149+18_1149+20del	NP_001317652.1:n.1149+18_1149+20del
XM_005245510.3:c.840+18_840+20del	XP_005245567.1:n.840+18_840+20del
XM_005245511.4:c.591+18_591+20del	XP_005245568.1:n.591+18_591+20del
XM_011510024.2:c.846+18_846+20del	XP_011508326.1:n.846+18_846+20del
XM_011510025.2:c.786+18_786+20del	XP_011508327.1:n.786+18_786+20del
XM_011510026.2:c.1149+18_1149+20del	XP_011508328.1:n.1149+18_1149+20del
XM_017002417.1:c.786+18_786+20del	XP_016857906.1:n.786+18_786+20del
XM_024450038.1:c.591+18_591+20del	XP_024305806.1:n.591+18_591+20del
XM_024450039.1:c.591+18_591+20del	XP_024305807.1:n.591+18_591+20del
NM_001330723.2:c.1149+18_1149+20del MANE Select	NP_001317652.1:n.1149+18_1149+20del
NM_030918.6:c.1149+18_1149+20del	NP_112180.4:n.1149+18_1149+20del