Canonical Allele Identifier: CA420747996

Gene: SNX27

Linked Data

• gnomAD v4: 1-151612291-C-T
• MyVariant Identifiers: chr1:g.151584767C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151612291C>T , CM000663.2:g.151612291C>T	GRCh38
NC_000001.10:g.151584767C>T , CM000663.1:g.151584767C>T	GRCh37
NC_000001.9:g.149851391C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368841.7:c.90C>T	ENSP00000357834.2:p.Cys30=
ENST00000368843.8:c.90C>T	ENSP00000357836.3:p.Cys30=
ENST00000458013.7:c.90C>T MANE Select	ENSP00000400333.2:p.Cys30=
ENST00000642376.1:c.90C>T	ENSP00000496645.1:p.Cys30=
ENST00000642479.1:c.90C>T	ENSP00000496775.1:p.Cys30=
ENST00000368841.6:c.90C>T	ENSP00000357834.2:p.Cys30=
ENST00000368843.7:c.90C>T	ENSP00000357836.3:p.Cys30=
ENST00000458013.6:c.90C>T	ENSP00000400333.2:p.Cys30=
NM_030918.5:c.90C>T	NP_112180.4:p.Cys30=
XM_005245509.1:c.90C>T	XP_005245566.1:p.Cys30=
XM_005245511.3:c.-338C>T	XP_005245568.1:n.-338C>T
XM_011510024.1:c.90C>T	XP_011508326.1:p.Cys30=
XM_011510025.1:c.90C>T	XP_011508327.1:p.Cys30=
XM_011510026.1:c.90C>T	XP_011508328.1:p.Cys30=
NM_001330723.1:c.90C>T	NP_001317652.1:p.Cys30=
XM_005245511.4:c.-338C>T	XP_005245568.1:n.-338C>T
XM_011510024.2:c.90C>T	XP_011508326.1:p.Cys30=
XM_011510025.2:c.90C>T	XP_011508327.1:p.Cys30=
XM_011510026.2:c.90C>T	XP_011508328.1:p.Cys30=
XM_017002417.1:c.90C>T	XP_016857906.1:p.Cys30=
XM_024450038.1:c.-237C>T	XP_024305806.1:n.-237C>T
NM_001330723.2:c.90C>T MANE Select	NP_001317652.1:p.Cys30=
NM_030918.6:c.90C>T	NP_112180.4:p.Cys30=