Canonical Allele Identifier: CA420752315

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151664997T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151692521T>C , CM000663.2:g.151692521T>C	GRCh38
NC_000001.10:g.151664997T>C , CM000663.1:g.151664997T>C	GRCh37
NC_000001.9:g.149931621T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368838.2:c.923T>C
ENST00000368841.7:c.*997T>C	ENSP00000357834.2:n.*997T>C
ENST00000368843.8:c.1326T>C	ENSP00000357836.3:p.Val442=
ENST00000458013.7:c.1326T>C MANE Select	ENSP00000400333.2:p.Val442=
ENST00000642349.1:c.1060T>C	ENSP00000494331.1:n.1060T>C
ENST00000642376.1:c.963T>C	ENSP00000496645.1:p.Val321=
ENST00000642479.1:c.*704T>C	ENSP00000496775.1:n.*704T>C
ENST00000643179.1:n.1134T>C
ENST00000643937.1:n.1004T>C
ENST00000644970.1:n.1324T>C
ENST00000647328.1:n.1047T>C
ENST00000647551.1:n.4775T>C
ENST00000368838.1:c.1047T>C	ENSP00000357831.1:p.Val349=
ENST00000368841.6:c.*997T>C	ENSP00000357834.2:n.*997T>C
ENST00000368843.7:c.1326T>C	ENSP00000357836.3:p.Val442=
ENST00000458013.6:c.1326T>C	ENSP00000400333.2:p.Val442=
NM_030918.5:c.1326T>C	NP_112180.4:p.Val442=
XM_005245509.1:c.1326T>C	XP_005245566.1:p.Val442=
XM_005245510.2:c.1017T>C	XP_005245567.1:p.Val339=
XM_005245511.3:c.768T>C	XP_005245568.1:p.Val256=
XM_011510024.1:c.1023T>C	XP_011508326.1:p.Val341=
XM_011510025.1:c.963T>C	XP_011508327.1:p.Val321=
NM_001330723.1:c.1326T>C	NP_001317652.1:p.Val442=
XM_005245510.3:c.1017T>C	XP_005245567.1:p.Val339=
XM_005245511.4:c.768T>C	XP_005245568.1:p.Val256=
XM_011510024.2:c.1023T>C	XP_011508326.1:p.Val341=
XM_011510025.2:c.963T>C	XP_011508327.1:p.Val321=
XM_017002417.1:c.963T>C	XP_016857906.1:p.Val321=
XM_024450038.1:c.768T>C	XP_024305806.1:p.Val256=
XM_024450039.1:c.768T>C	XP_024305807.1:p.Val256=
NM_001330723.2:c.1326T>C MANE Select	NP_001317652.1:p.Val442=
NM_030918.6:c.1326T>C	NP_112180.4:p.Val442=