Canonical Allele Identifier: CA341972243

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151665002C>T (hg19) ; chr1:g.151692526C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692526C>T , CM000663.2:g.151692526C>T	GRCh38
NC_000001.10:g.151665002C>T , CM000663.1:g.151665002C>T	GRCh37
NC_000001.9:g.149931626C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.928C>T
ENST00000368841.7:c.*1002C>T	ENSP00000357834.2:n.*1002C>T
ENST00000368843.8:c.1331C>T	ENSP00000357836.3:p.Thr444Ile
ENST00000458013.7:c.1331C>T MANE Select	ENSP00000400333.2:p.Thr444Ile
ENST00000642349.1:c.1065C>T	ENSP00000494331.1:n.1065C>T
ENST00000642376.1:c.968C>T	ENSP00000496645.1:p.Thr323Ile
ENST00000642479.1:c.*709C>T	ENSP00000496775.1:n.*709C>T
ENST00000643179.1:n.1139C>T
ENST00000643937.1:n.1009C>T
ENST00000644970.1:n.1329C>T
ENST00000647328.1:n.1052C>T
ENST00000647551.1:n.4780C>T
ENST00000368838.1:c.1052C>T	ENSP00000357831.1:p.Thr351Ile
ENST00000368841.6:c.*1002C>T	ENSP00000357834.2:n.*1002C>T
ENST00000368843.7:c.1331C>T	ENSP00000357836.3:p.Thr444Ile
ENST00000458013.6:c.1331C>T	ENSP00000400333.2:p.Thr444Ile
NM_030918.5:c.1331C>T	NP_112180.4:p.Thr444Ile
XM_005245509.1:c.1331C>T	XP_005245566.1:p.Thr444Ile
XM_005245510.2:c.1022C>T	XP_005245567.1:p.Thr341Ile
XM_005245511.3:c.773C>T	XP_005245568.1:p.Thr258Ile
XM_011510024.1:c.1028C>T	XP_011508326.1:p.Thr343Ile
XM_011510025.1:c.968C>T	XP_011508327.1:p.Thr323Ile
NM_001330723.1:c.1331C>T	NP_001317652.1:p.Thr444Ile
XM_005245510.3:c.1022C>T	XP_005245567.1:p.Thr341Ile
XM_005245511.4:c.773C>T	XP_005245568.1:p.Thr258Ile
XM_011510024.2:c.1028C>T	XP_011508326.1:p.Thr343Ile
XM_011510025.2:c.968C>T	XP_011508327.1:p.Thr323Ile
XM_017002417.1:c.968C>T	XP_016857906.1:p.Thr323Ile
XM_024450038.1:c.773C>T	XP_024305806.1:p.Thr258Ile
XM_024450039.1:c.773C>T	XP_024305807.1:p.Thr258Ile
NM_001330723.2:c.1331C>T MANE Select	NP_001317652.1:p.Thr444Ile
NM_030918.6:c.1331C>T	NP_112180.4:p.Thr444Ile