Canonical Allele Identifier: CA341972235

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151665001A>T (hg19) ; chr1:g.151692525A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692525A>T , CM000663.2:g.151692525A>T	GRCh38
NC_000001.10:g.151665001A>T , CM000663.1:g.151665001A>T	GRCh37
NC_000001.9:g.149931625A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.927A>T
ENST00000368841.7:c.*1001A>T	ENSP00000357834.2:n.*1001A>T
ENST00000368843.8:c.1330A>T	ENSP00000357836.3:p.Thr444Ser
ENST00000458013.7:c.1330A>T MANE Select	ENSP00000400333.2:p.Thr444Ser
ENST00000642349.1:c.1064A>T	ENSP00000494331.1:n.1064A>T
ENST00000642376.1:c.967A>T	ENSP00000496645.1:p.Thr323Ser
ENST00000642479.1:c.*708A>T	ENSP00000496775.1:n.*708A>T
ENST00000643179.1:n.1138A>T
ENST00000643937.1:n.1008A>T
ENST00000644970.1:n.1328A>T
ENST00000647328.1:n.1051A>T
ENST00000647551.1:n.4779A>T
ENST00000368838.1:c.1051A>T	ENSP00000357831.1:p.Thr351Ser
ENST00000368841.6:c.*1001A>T	ENSP00000357834.2:n.*1001A>T
ENST00000368843.7:c.1330A>T	ENSP00000357836.3:p.Thr444Ser
ENST00000458013.6:c.1330A>T	ENSP00000400333.2:p.Thr444Ser
NM_030918.5:c.1330A>T	NP_112180.4:p.Thr444Ser
XM_005245509.1:c.1330A>T	XP_005245566.1:p.Thr444Ser
XM_005245510.2:c.1021A>T	XP_005245567.1:p.Thr341Ser
XM_005245511.3:c.772A>T	XP_005245568.1:p.Thr258Ser
XM_011510024.1:c.1027A>T	XP_011508326.1:p.Thr343Ser
XM_011510025.1:c.967A>T	XP_011508327.1:p.Thr323Ser
NM_001330723.1:c.1330A>T	NP_001317652.1:p.Thr444Ser
XM_005245510.3:c.1021A>T	XP_005245567.1:p.Thr341Ser
XM_005245511.4:c.772A>T	XP_005245568.1:p.Thr258Ser
XM_011510024.2:c.1027A>T	XP_011508326.1:p.Thr343Ser
XM_011510025.2:c.967A>T	XP_011508327.1:p.Thr323Ser
XM_017002417.1:c.967A>T	XP_016857906.1:p.Thr323Ser
XM_024450038.1:c.772A>T	XP_024305806.1:p.Thr258Ser
XM_024450039.1:c.772A>T	XP_024305807.1:p.Thr258Ser
NM_001330723.2:c.1330A>T MANE Select	NP_001317652.1:p.Thr444Ser
NM_030918.6:c.1330A>T	NP_112180.4:p.Thr444Ser