Canonical Allele Identifier: CA1093668

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692899T>C , CM000663.2:g.151692899T>C	GRCh38
NC_000001.10:g.151665375T>C , CM000663.1:g.151665375T>C	GRCh37
NC_000001.9:g.149931999T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368838.2:c.987-12T>C
ENST00000368841.7:c.*1061-12T>C	ENSP00000357834.2:n.*1061-12T>C
ENST00000368843.8:c.1390-12T>C	ENSP00000357836.3:n.1390-12T>C
ENST00000458013.7:c.1390-12T>C MANE Select	ENSP00000400333.2:n.1390-12T>C
ENST00000642349.1:c.1124-12T>C	ENSP00000494331.1:n.1124-12T>C
ENST00000642376.1:c.1027-12T>C	ENSP00000496645.1:n.1027-12T>C
ENST00000642479.1:c.*768-12T>C	ENSP00000496775.1:n.*768-12T>C
ENST00000643179.1:n.1198-12T>C
ENST00000643937.1:n.1068-12T>C
ENST00000644970.1:n.1388-12T>C
ENST00000647328.1:n.1111-12T>C
ENST00000647551.1:n.4839-12T>C
ENST00000368838.1:c.1111-12T>C	ENSP00000357831.1:n.1111-12T>C
ENST00000368841.6:c.*1061-12T>C	ENSP00000357834.2:n.*1061-12T>C
ENST00000368843.7:c.1390-12T>C	ENSP00000357836.3:n.1390-12T>C
ENST00000458013.6:c.1390-12T>C	ENSP00000400333.2:n.1390-12T>C
NM_030918.5:c.1390-12T>C	NP_112180.4:n.1390-12T>C
XM_005245509.1:c.1390-12T>C	XP_005245566.1:n.1390-12T>C
XM_005245510.2:c.1081-12T>C	XP_005245567.1:n.1081-12T>C
XM_005245511.3:c.832-12T>C	XP_005245568.1:n.832-12T>C
XM_011510024.1:c.1087-12T>C	XP_011508326.1:n.1087-12T>C
XM_011510025.1:c.1027-12T>C	XP_011508327.1:n.1027-12T>C
NM_001330723.1:c.1390-12T>C	NP_001317652.1:n.1390-12T>C
XM_005245510.3:c.1081-12T>C	XP_005245567.1:n.1081-12T>C
XM_005245511.4:c.832-12T>C	XP_005245568.1:n.832-12T>C
XM_011510024.2:c.1087-12T>C	XP_011508326.1:n.1087-12T>C
XM_011510025.2:c.1027-12T>C	XP_011508327.1:n.1027-12T>C
XM_017002417.1:c.1027-12T>C	XP_016857906.1:n.1027-12T>C
XM_024450038.1:c.832-12T>C	XP_024305806.1:n.832-12T>C
XM_024450039.1:c.832-12T>C	XP_024305807.1:n.832-12T>C
NM_001330723.2:c.1390-12T>C MANE Select	NP_001317652.1:n.1390-12T>C
NM_030918.6:c.1390-12T>C	NP_112180.4:n.1390-12T>C