Canonical Allele Identifier: CA341972269

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151665008T>C (hg19) ; chr1:g.151692532T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692532T>C , CM000663.2:g.151692532T>C	GRCh38
NC_000001.10:g.151665008T>C , CM000663.1:g.151665008T>C	GRCh37
NC_000001.9:g.149931632T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.934T>C
ENST00000368841.7:c.*1008T>C	ENSP00000357834.2:n.*1008T>C
ENST00000368843.8:c.1337T>C	ENSP00000357836.3:p.Ile446Thr
ENST00000458013.7:c.1337T>C MANE Select	ENSP00000400333.2:p.Ile446Thr
ENST00000642349.1:c.1071T>C	ENSP00000494331.1:n.1071T>C
ENST00000642376.1:c.974T>C	ENSP00000496645.1:p.Ile325Thr
ENST00000642479.1:c.*715T>C	ENSP00000496775.1:n.*715T>C
ENST00000643179.1:n.1145T>C
ENST00000643937.1:n.1015T>C
ENST00000644970.1:n.1335T>C
ENST00000647328.1:n.1058T>C
ENST00000647551.1:n.4786T>C
ENST00000368838.1:c.1058T>C	ENSP00000357831.1:p.Ile353Thr
ENST00000368841.6:c.*1008T>C	ENSP00000357834.2:n.*1008T>C
ENST00000368843.7:c.1337T>C	ENSP00000357836.3:p.Ile446Thr
ENST00000458013.6:c.1337T>C	ENSP00000400333.2:p.Ile446Thr
NM_030918.5:c.1337T>C	NP_112180.4:p.Ile446Thr
XM_005245509.1:c.1337T>C	XP_005245566.1:p.Ile446Thr
XM_005245510.2:c.1028T>C	XP_005245567.1:p.Ile343Thr
XM_005245511.3:c.779T>C	XP_005245568.1:p.Ile260Thr
XM_011510024.1:c.1034T>C	XP_011508326.1:p.Ile345Thr
XM_011510025.1:c.974T>C	XP_011508327.1:p.Ile325Thr
NM_001330723.1:c.1337T>C	NP_001317652.1:p.Ile446Thr
XM_005245510.3:c.1028T>C	XP_005245567.1:p.Ile343Thr
XM_005245511.4:c.779T>C	XP_005245568.1:p.Ile260Thr
XM_011510024.2:c.1034T>C	XP_011508326.1:p.Ile345Thr
XM_011510025.2:c.974T>C	XP_011508327.1:p.Ile325Thr
XM_017002417.1:c.974T>C	XP_016857906.1:p.Ile325Thr
XM_024450038.1:c.779T>C	XP_024305806.1:p.Ile260Thr
XM_024450039.1:c.779T>C	XP_024305807.1:p.Ile260Thr
NM_001330723.2:c.1337T>C MANE Select	NP_001317652.1:p.Ile446Thr
NM_030918.6:c.1337T>C	NP_112180.4:p.Ile446Thr