Canonical Allele Identifier: CA420752318

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151665003A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692527A>C , CM000663.2:g.151692527A>C	GRCh38
NC_000001.10:g.151665003A>C , CM000663.1:g.151665003A>C	GRCh37
NC_000001.9:g.149931627A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.929A>C
ENST00000368841.7:c.*1003A>C	ENSP00000357834.2:n.*1003A>C
ENST00000368843.8:c.1332A>C	ENSP00000357836.3:p.Thr444=
ENST00000458013.7:c.1332A>C MANE Select	ENSP00000400333.2:p.Thr444=
ENST00000642349.1:c.1066A>C	ENSP00000494331.1:n.1066A>C
ENST00000642376.1:c.969A>C	ENSP00000496645.1:p.Thr323=
ENST00000642479.1:c.*710A>C	ENSP00000496775.1:n.*710A>C
ENST00000643179.1:n.1140A>C
ENST00000643937.1:n.1010A>C
ENST00000644970.1:n.1330A>C
ENST00000647328.1:n.1053A>C
ENST00000647551.1:n.4781A>C
ENST00000368838.1:c.1053A>C	ENSP00000357831.1:p.Thr351=
ENST00000368841.6:c.*1003A>C	ENSP00000357834.2:n.*1003A>C
ENST00000368843.7:c.1332A>C	ENSP00000357836.3:p.Thr444=
ENST00000458013.6:c.1332A>C	ENSP00000400333.2:p.Thr444=
NM_030918.5:c.1332A>C	NP_112180.4:p.Thr444=
XM_005245509.1:c.1332A>C	XP_005245566.1:p.Thr444=
XM_005245510.2:c.1023A>C	XP_005245567.1:p.Thr341=
XM_005245511.3:c.774A>C	XP_005245568.1:p.Thr258=
XM_011510024.1:c.1029A>C	XP_011508326.1:p.Thr343=
XM_011510025.1:c.969A>C	XP_011508327.1:p.Thr323=
NM_001330723.1:c.1332A>C	NP_001317652.1:p.Thr444=
XM_005245510.3:c.1023A>C	XP_005245567.1:p.Thr341=
XM_005245511.4:c.774A>C	XP_005245568.1:p.Thr258=
XM_011510024.2:c.1029A>C	XP_011508326.1:p.Thr343=
XM_011510025.2:c.969A>C	XP_011508327.1:p.Thr323=
XM_017002417.1:c.969A>C	XP_016857906.1:p.Thr323=
XM_024450038.1:c.774A>C	XP_024305806.1:p.Thr258=
XM_024450039.1:c.774A>C	XP_024305807.1:p.Thr258=
NM_001330723.2:c.1332A>C MANE Select	NP_001317652.1:p.Thr444=
NM_030918.6:c.1332A>C	NP_112180.4:p.Thr444=