Canonical Allele Identifier: CA12254861

Gene: SNX9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157944003C>T , CM000668.2:g.157944003C>T	GRCh38
NC_000006.11:g.158365035C>T , CM000668.1:g.158365035C>T	GRCh37
NC_000006.10:g.158285023C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392185.8:c.*1165C>T MANE Select	ENSP00000376024.3:n.*1165C>T
ENST00000679691.1:c.*1165C>T	ENSP00000505486.1:n.*1165C>T
ENST00000679790.1:c.*2349C>T	ENSP00000506493.1:n.*2349C>T
ENST00000679814.1:c.*616-25C>T	ENSP00000506326.1:n.*616-25C>T
ENST00000680078.1:c.*1165C>T	ENSP00000505598.1:n.*1165C>T
ENST00000680089.1:n.6618C>T
ENST00000680464.1:n.5302C>T
ENST00000680495.1:c.*1165C>T	ENSP00000505186.1:n.*1165C>T
ENST00000680680.1:n.4241C>T
ENST00000680863.1:c.*1165C>T	ENSP00000505291.1:n.*1165C>T
ENST00000680974.1:n.4275C>T
ENST00000681138.1:c.*1165C>T	ENSP00000505392.1:n.*1165C>T
ENST00000681186.1:c.*1197C>T	ENSP00000506632.1:n.*1197C>T
ENST00000681469.1:n.2605C>T
ENST00000681651.1:c.*2894C>T	ENSP00000505173.1:n.*2894C>T
ENST00000392185.7:c.*1165C>T	ENSP00000376024.3:n.*1165C>T
ENST00000611124.1:c.2950C>T	ENSP00000482087.1:n.2950C>T
NM_016224.4:c.*1165C>T	NP_057308.1:n.*1165C>T
XM_005267015.1:c.*1165C>T	XP_005267072.1:n.*1165C>T
XM_011535886.1:c.*1165C>T	XP_011534188.1:n.*1165C>T
XM_005267015.2:c.*1165C>T	XP_005267072.1:n.*1165C>T
NM_016224.5:c.*1165C>T MANE Select	NP_057308.1:n.*1165C>T