Canonical Allele Identifier: CA2285168908

Gene: CIDEA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12274698T>A , CM000680.2:g.12274698T>A	GRCh38
NC_000018.9:g.12274697T>A , CM000680.1:g.12274697T>A	GRCh37
NC_000018.8:g.12264697T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320477.10:c.512+424T>A MANE Select	ENSP00000320209.8:n.512+424T>A
ENST00000320477.9:c.512+424T>A	ENSP00000320209.8:n.512+424T>A
ENST00000520620.1:n.525-2425T>A
ENST00000521296.5:n.729+424T>A
ENST00000522713.5:c.*711+424T>A	ENSP00000429238.1:n.*711+424T>A
NM_001279.3:c.512+424T>A	NP_001270.1:n.512+424T>A
NR_036468.1:n.1070+424T>A
XM_011525602.1:c.215+424T>A	XP_011523904.1:n.215+424T>A
NM_001318383.1:c.614+424T>A	NP_001305312.1:n.614+424T>A
NR_134607.1:n.1337+424T>A
NM_001279.4:c.512+424T>A MANE Select	NP_001270.1:n.512+424T>A
NM_001318383.2:c.614+424T>A	NP_001305312.1:n.614+424T>A
NR_134607.2:n.1337+424T>A