Canonical Allele Identifier: CA2479658058

Gene: SNX27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612232C= , CM000663.2:g.151612232C=	GRCh38
NC_000001.10:g.151584708C= , CM000663.1:g.151584708C=	GRCh37
NC_000001.9:g.149851332C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.31C=	ENSP00000357834.2:p.Pro11=
ENST00000368843.8:c.31C=	ENSP00000357836.3:p.Pro11=
ENST00000458013.7:c.31C= MANE Select	ENSP00000400333.2:p.Pro11=
ENST00000642376.1:c.31C=	ENSP00000496645.1:p.Pro11=
ENST00000642479.1:c.31C=	ENSP00000496775.1:p.Pro11=
ENST00000368841.6:c.31C=	ENSP00000357834.2:p.Pro11=
ENST00000368843.7:c.31C=	ENSP00000357836.3:p.Pro11=
ENST00000458013.6:c.31C=	ENSP00000400333.2:p.Pro11=
NM_030918.5:c.31C=	NP_112180.4:p.Pro11=
XM_005245509.1:c.31C=	XP_005245566.1:p.Pro11=
XM_005245511.3:c.-397C=	XP_005245568.1:n.-397C=
XM_011510024.1:c.31C=	XP_011508326.1:p.Pro11=
XM_011510025.1:c.31C=	XP_011508327.1:p.Pro11=
XM_011510026.1:c.31C=	XP_011508328.1:p.Pro11=
NM_001330723.1:c.31C=	NP_001317652.1:p.Pro11=
XM_005245511.4:c.-397C=	XP_005245568.1:n.-397C=
XM_011510024.2:c.31C=	XP_011508326.1:p.Pro11=
XM_011510025.2:c.31C=	XP_011508327.1:p.Pro11=
XM_011510026.2:c.31C=	XP_011508328.1:p.Pro11=
XM_017002417.1:c.31C=	XP_016857906.1:p.Pro11=
XM_024450038.1:c.-296C=	XP_024305806.1:n.-296C=
NM_001330723.2:c.31C= MANE Select	NP_001317652.1:p.Pro11=
NM_030918.6:c.31C=	NP_112180.4:p.Pro11=