Canonical Allele Identifier: CA341973641

Gene: SNX27

Linked Data

• MyVariant Identifiers: chr1:g.151584738G>C (hg19) ; chr1:g.151612262G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612262G>C , CM000663.2:g.151612262G>C	GRCh38
NC_000001.10:g.151584738G>C , CM000663.1:g.151584738G>C	GRCh37
NC_000001.9:g.149851362G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.61G>C	ENSP00000357834.2:p.Gly21Arg
ENST00000368843.8:c.61G>C	ENSP00000357836.3:p.Gly21Arg
ENST00000458013.7:c.61G>C MANE Select	ENSP00000400333.2:p.Gly21Arg
ENST00000642376.1:c.61G>C	ENSP00000496645.1:p.Gly21Arg
ENST00000642479.1:c.61G>C	ENSP00000496775.1:p.Gly21Arg
ENST00000368841.6:c.61G>C	ENSP00000357834.2:p.Gly21Arg
ENST00000368843.7:c.61G>C	ENSP00000357836.3:p.Gly21Arg
ENST00000458013.6:c.61G>C	ENSP00000400333.2:p.Gly21Arg
NM_030918.5:c.61G>C	NP_112180.4:p.Gly21Arg
XM_005245509.1:c.61G>C	XP_005245566.1:p.Gly21Arg
XM_005245511.3:c.-367G>C	XP_005245568.1:n.-367G>C
XM_011510024.1:c.61G>C	XP_011508326.1:p.Gly21Arg
XM_011510025.1:c.61G>C	XP_011508327.1:p.Gly21Arg
XM_011510026.1:c.61G>C	XP_011508328.1:p.Gly21Arg
NM_001330723.1:c.61G>C	NP_001317652.1:p.Gly21Arg
XM_005245511.4:c.-367G>C	XP_005245568.1:n.-367G>C
XM_011510024.2:c.61G>C	XP_011508326.1:p.Gly21Arg
XM_011510025.2:c.61G>C	XP_011508327.1:p.Gly21Arg
XM_011510026.2:c.61G>C	XP_011508328.1:p.Gly21Arg
XM_017002417.1:c.61G>C	XP_016857906.1:p.Gly21Arg
XM_024450038.1:c.-266G>C	XP_024305806.1:n.-266G>C
NM_001330723.2:c.61G>C MANE Select	NP_001317652.1:p.Gly21Arg
NM_030918.6:c.61G>C	NP_112180.4:p.Gly21Arg