Canonical Allele Identifier: CA242020391

Gene: CRADD CRADD-AS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93726563C>G , CM000674.2:g.93726563C>G	GRCh38
NC_000012.11:g.94120339C>G , CM000674.1:g.94120339C>G	GRCh37
NC_000012.10:g.92644470C>G	NCBI36
NG_032159.1:g.54189C>G
NG_032159.2:g.54189C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.298+47491C>G (CRADD) MANE Select	ENSP00000327647.3:n.298+47491C>G
ENST00000332896.7:c.298+47491C>G (CRADD)	ENSP00000327647.3:n.298+47491C>G
ENST00000542893.2:c.298+47491C>G (CRADD)	ENSP00000439068.2:n.298+47491C>G
ENST00000548483.5:c.298+47491C>G (CRADD)	ENSP00000448685.1:n.298+47491C>G
ENST00000549615.5:n.402+47491C>G (CRADD)
ENST00000551065.5:c.298+47491C>G (CRADD)	ENSP00000448425.1:n.298+47491C>G
ENST00000552033.5:c.299-11841C>G (CRADD)	ENSP00000449664.1:n.299-11841C>G
ENST00000552983.5:c.299-11637C>G (CRADD)	ENSP00000449570.1:n.299-11637C>G
NM_003805.3:c.298+47491C>G (CRADD)	NP_003796.1:n.298+47491C>G
NR_110092.1:n.294+9002G>C (CRADD-AS1)
NR_110093.1:n.294+9002G>C (CRADD-AS1)
XM_005269211.3:c.298+47491C>G (CRADD)	XP_005269268.1:n.298+47491C>G
NM_001320099.1:c.298+47491C>G (CRADD)	NP_001307028.1:n.298+47491C>G
NM_001320100.1:c.298+47491C>G (CRADD)	NP_001307029.1:n.298+47491C>G
NM_001320101.1:c.299-11841C>G (CRADD)	NP_001307030.1:n.299-11841C>G
NM_001330126.1:c.299-11637C>G (CRADD)	NP_001317055.1:n.299-11637C>G
NM_003805.4:c.298+47491C>G (CRADD)	NP_003796.1:n.298+47491C>G
NR_135147.1:n.406+47491C>G (CRADD)
XM_017020143.2:c.298+47491C>G (CRADD)	XP_016875632.1:n.298+47491C>G
XM_017020144.1:c.298+47491C>G (CRADD)	XP_016875633.1:n.298+47491C>G
XM_024449252.1:c.299-11637C>G (CRADD)	XP_024305020.1:n.299-11637C>G
XR_001748908.1:n.431+47491C>G (CRADD)
XR_001748909.1:n.429+47491C>G (CRADD)
XR_001748910.1:n.429+47491C>G (CRADD)
NM_003805.5:c.298+47491C>G (CRADD) MANE Select	NP_003796.1:n.298+47491C>G
NM_001320101.2:c.299-11841C>G (CRADD)	NP_001307030.1:n.299-11841C>G
NM_001320099.2:c.298+47491C>G (CRADD)	NP_001307028.1:n.298+47491C>G
NM_001320100.2:c.298+47491C>G (CRADD)	NP_001307029.1:n.298+47491C>G
NM_001320101.3:c.299-11841C>G (CRADD)	NP_001307030.1:n.299-11841C>G
NR_135147.2:n.402+47491C>G (CRADD)