Canonical Allele Identifier: CA341958310

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151658239A>G , CM000663.2:g.151658239A>G	GRCh38
NC_000001.10:g.151630715A>G , CM000663.1:g.151630715A>G	GRCh37
NC_000001.9:g.149897339A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.145A>G
ENST00000368841.7:c.*219A>G	ENSP00000357834.2:n.*219A>G
ENST00000368843.8:c.548A>G	ENSP00000357836.3:p.Tyr183Cys
ENST00000458013.7:c.548A>G MANE Select	ENSP00000400333.2:p.Tyr183Cys
ENST00000642349.1:c.282A>G	ENSP00000494331.1:n.282A>G
ENST00000642376.1:c.185A>G	ENSP00000496645.1:p.Tyr62Cys
ENST00000642479.1:c.316A>G	ENSP00000496775.1:p.Ile106Val
ENST00000642582.1:n.264A>G
ENST00000643179.1:n.356A>G
ENST00000643814.1:n.269A>G
ENST00000643845.1:n.5A>G
ENST00000644113.1:n.232A>G
ENST00000644970.1:n.546A>G
ENST00000647328.1:n.269A>G
ENST00000368838.1:c.269A>G	ENSP00000357831.1:p.Tyr90Cys
ENST00000368841.6:c.*219A>G	ENSP00000357834.2:n.*219A>G
ENST00000368843.7:c.548A>G	ENSP00000357836.3:p.Tyr183Cys
ENST00000458013.6:c.548A>G	ENSP00000400333.2:p.Tyr183Cys
NM_030918.5:c.548A>G	NP_112180.4:p.Tyr183Cys
XM_005245509.1:c.548A>G	XP_005245566.1:p.Tyr183Cys
XM_005245510.2:c.239A>G	XP_005245567.1:p.Tyr80Cys
XM_005245511.3:c.-11A>G	XP_005245568.1:n.-11A>G
XM_011510024.1:c.245A>G	XP_011508326.1:p.Tyr82Cys
XM_011510025.1:c.185A>G	XP_011508327.1:p.Tyr62Cys
XM_011510026.1:c.548A>G	XP_011508328.1:p.Tyr183Cys
NM_001330723.1:c.548A>G	NP_001317652.1:p.Tyr183Cys
XM_005245510.3:c.239A>G	XP_005245567.1:p.Tyr80Cys
XM_005245511.4:c.-11A>G	XP_005245568.1:n.-11A>G
XM_011510024.2:c.245A>G	XP_011508326.1:p.Tyr82Cys
XM_011510025.2:c.185A>G	XP_011508327.1:p.Tyr62Cys
XM_011510026.2:c.548A>G	XP_011508328.1:p.Tyr183Cys
XM_017002417.1:c.185A>G	XP_016857906.1:p.Tyr62Cys
XM_024450038.1:c.-11A>G	XP_024305806.1:n.-11A>G
XM_024450039.1:c.-11A>G	XP_024305807.1:n.-11A>G
NM_001330723.2:c.548A>G MANE Select	NP_001317652.1:p.Tyr183Cys
NM_030918.6:c.548A>G	NP_112180.4:p.Tyr183Cys