Canonical Allele Identifier: CA1093639

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692485C>G , CM000663.2:g.151692485C>G	GRCh38
NC_000001.10:g.151664961C>G , CM000663.1:g.151664961C>G	GRCh37
NC_000001.9:g.149931585C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.887C>G
ENST00000368841.7:c.*961C>G	ENSP00000357834.2:n.*961C>G
ENST00000368843.8:c.1290C>G	ENSP00000357836.3:p.Pro430=
ENST00000458013.7:c.1290C>G MANE Select	ENSP00000400333.2:p.Pro430=
ENST00000642349.1:c.1024C>G	ENSP00000494331.1:n.1024C>G
ENST00000642376.1:c.927C>G	ENSP00000496645.1:p.Pro309=
ENST00000642479.1:c.*668C>G	ENSP00000496775.1:n.*668C>G
ENST00000643179.1:n.1098C>G
ENST00000643937.1:n.968C>G
ENST00000644970.1:n.1288C>G
ENST00000647328.1:n.1011C>G
ENST00000647551.1:n.4739C>G
ENST00000368838.1:c.1011C>G	ENSP00000357831.1:p.Pro337=
ENST00000368841.6:c.*961C>G	ENSP00000357834.2:n.*961C>G
ENST00000368843.7:c.1290C>G	ENSP00000357836.3:p.Pro430=
ENST00000458013.6:c.1290C>G	ENSP00000400333.2:p.Pro430=
NM_030918.5:c.1290C>G	NP_112180.4:p.Pro430=
XM_005245509.1:c.1290C>G	XP_005245566.1:p.Pro430=
XM_005245510.2:c.981C>G	XP_005245567.1:p.Pro327=
XM_005245511.3:c.732C>G	XP_005245568.1:p.Pro244=
XM_011510024.1:c.987C>G	XP_011508326.1:p.Pro329=
XM_011510025.1:c.927C>G	XP_011508327.1:p.Pro309=
NM_001330723.1:c.1290C>G	NP_001317652.1:p.Pro430=
XM_005245510.3:c.981C>G	XP_005245567.1:p.Pro327=
XM_005245511.4:c.732C>G	XP_005245568.1:p.Pro244=
XM_011510024.2:c.987C>G	XP_011508326.1:p.Pro329=
XM_011510025.2:c.927C>G	XP_011508327.1:p.Pro309=
XM_017002417.1:c.927C>G	XP_016857906.1:p.Pro309=
XM_024450038.1:c.732C>G	XP_024305806.1:p.Pro244=
XM_024450039.1:c.732C>G	XP_024305807.1:p.Pro244=
NM_001330723.2:c.1290C>G MANE Select	NP_001317652.1:p.Pro430=
NM_030918.6:c.1290C>G	NP_112180.4:p.Pro430=