Canonical Allele Identifier: CA420751848

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151683433A>G , CM000663.2:g.151683433A>G	GRCh38
NC_000001.10:g.151655909A>G , CM000663.1:g.151655909A>G	GRCh37
NC_000001.9:g.149922533A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.824A>G
ENST00000368841.7:c.*898A>G	ENSP00000357834.2:n.*898A>G
ENST00000368843.8:c.1227A>G	ENSP00000357836.3:p.Arg409=
ENST00000458013.7:c.1227A>G MANE Select	ENSP00000400333.2:p.Arg409=
ENST00000642349.1:c.961A>G	ENSP00000494331.1:n.961A>G
ENST00000642376.1:c.864A>G	ENSP00000496645.1:p.Arg288=
ENST00000642479.1:c.*605A>G	ENSP00000496775.1:n.*605A>G
ENST00000643179.1:n.1035A>G
ENST00000643937.1:n.905A>G
ENST00000644113.1:n.911A>G
ENST00000644970.1:n.1225A>G
ENST00000647328.1:n.948A>G
ENST00000647551.1:n.4676A>G
ENST00000368838.1:c.948A>G	ENSP00000357831.1:p.Arg316=
ENST00000368841.6:c.*898A>G	ENSP00000357834.2:n.*898A>G
ENST00000368843.7:c.1227A>G	ENSP00000357836.3:p.Arg409=
ENST00000458013.6:c.1227A>G	ENSP00000400333.2:p.Arg409=
NM_030918.5:c.1227A>G	NP_112180.4:p.Arg409=
XM_005245509.1:c.1227A>G	XP_005245566.1:p.Arg409=
XM_005245510.2:c.918A>G	XP_005245567.1:p.Arg306=
XM_005245511.3:c.669A>G	XP_005245568.1:p.Arg223=
XM_011510024.1:c.924A>G	XP_011508326.1:p.Arg308=
XM_011510025.1:c.864A>G	XP_011508327.1:p.Arg288=
NM_001330723.1:c.1227A>G	NP_001317652.1:p.Arg409=
XM_005245510.3:c.918A>G	XP_005245567.1:p.Arg306=
XM_005245511.4:c.669A>G	XP_005245568.1:p.Arg223=
XM_011510024.2:c.924A>G	XP_011508326.1:p.Arg308=
XM_011510025.2:c.864A>G	XP_011508327.1:p.Arg288=
XM_017002417.1:c.864A>G	XP_016857906.1:p.Arg288=
XM_024450038.1:c.669A>G	XP_024305806.1:p.Arg223=
XM_024450039.1:c.669A>G	XP_024305807.1:p.Arg223=
NM_001330723.2:c.1227A>G MANE Select	NP_001317652.1:p.Arg409=
NM_030918.6:c.1227A>G	NP_112180.4:p.Arg409=