Canonical Allele Identifier: CA1093396

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151638927G>C , CM000663.2:g.151638927G>C	GRCh38
NC_000001.10:g.151611403G>C , CM000663.1:g.151611403G>C	GRCh37
NC_000001.9:g.149878027G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.*22G>C	ENSP00000357834.2:n.*22G>C
ENST00000368843.8:c.351G>C	ENSP00000357836.3:p.Val117=
ENST00000458013.7:c.351G>C MANE Select	ENSP00000400333.2:p.Val117=
ENST00000642349.1:c.85G>C	ENSP00000494331.1:n.85G>C
ENST00000642376.1:c.181-19308G>C	ENSP00000496645.1:n.181-19308G>C
ENST00000642479.1:c.312-19308G>C	ENSP00000496775.1:n.312-19308G>C
ENST00000642582.1:n.67G>C
ENST00000643179.1:n.159G>C
ENST00000643814.1:n.72G>C
ENST00000644113.1:n.35G>C
ENST00000644970.1:n.542-19308G>C
ENST00000647328.1:n.72G>C
ENST00000368838.1:c.72G>C	ENSP00000357831.1:p.Val24=
ENST00000368841.6:c.*22G>C	ENSP00000357834.2:n.*22G>C
ENST00000368843.7:c.351G>C	ENSP00000357836.3:p.Val117=
ENST00000458013.6:c.351G>C	ENSP00000400333.2:p.Val117=
NM_030918.5:c.351G>C	NP_112180.4:p.Val117=
XM_005245509.1:c.351G>C	XP_005245566.1:p.Val117=
XM_005245510.2:c.42G>C	XP_005245567.1:p.Val14=
XM_005245511.3:c.-208G>C	XP_005245568.1:n.-208G>C
XM_011510024.1:c.241-19308G>C	XP_011508326.1:n.241-19308G>C
XM_011510025.1:c.181-19308G>C	XP_011508327.1:n.181-19308G>C
XM_011510026.1:c.351G>C	XP_011508328.1:p.Val117=
NM_001330723.1:c.351G>C	NP_001317652.1:p.Val117=
XM_005245510.3:c.42G>C	XP_005245567.1:p.Val14=
XM_005245511.4:c.-208G>C	XP_005245568.1:n.-208G>C
XM_011510024.2:c.241-19308G>C	XP_011508326.1:n.241-19308G>C
XM_011510025.2:c.181-19308G>C	XP_011508327.1:n.181-19308G>C
XM_011510026.2:c.351G>C	XP_011508328.1:p.Val117=
XM_017002417.1:c.181-19308G>C	XP_016857906.1:n.181-19308G>C
XM_024450038.1:c.-15-19308G>C	XP_024305806.1:n.-15-19308G>C
XM_024450039.1:c.-15-19308G>C	XP_024305807.1:n.-15-19308G>C
NM_001330723.2:c.351G>C MANE Select	NP_001317652.1:p.Val117=
NM_030918.6:c.351G>C	NP_112180.4:p.Val117=