Canonical Allele Identifier: CA386142337

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243766C>A (hg19) ; chr12:g.93849990C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93849990C>A , CM000674.2:g.93849990C>A	GRCh38
NC_000012.11:g.94243766C>A , CM000674.1:g.94243766C>A	GRCh37
NC_000012.10:g.92767897C>A	NCBI36
NG_032159.1:g.177616C>A
NG_032159.2:g.177616C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.319C>A MANE Select	ENSP00000327647.3:p.Pro107Thr
ENST00000332896.7:c.319C>A	ENSP00000327647.3:p.Pro107Thr
ENST00000542893.2:c.319C>A	ENSP00000439068.2:p.Pro107Thr
ENST00000548330.1:n.704C>A
ENST00000548483.5:c.299-44060C>A	ENSP00000448685.1:n.299-44060C>A
ENST00000550030.1:n.119C>A
ENST00000551065.5:c.299-9329C>A	ENSP00000448425.1:n.299-9329C>A
ENST00000609189.1:n.95C>A
NM_003805.3:c.319C>A	NP_003796.1:p.Pro107Thr
XM_005269211.3:c.299-44060C>A	XP_005269268.1:n.299-44060C>A
NM_001320099.1:c.319C>A	NP_001307028.1:p.Pro107Thr
NM_001320100.1:c.299-44060C>A	NP_001307029.1:n.299-44060C>A
NM_003805.4:c.319C>A	NP_003796.1:p.Pro107Thr
NR_135147.1:n.407-9329C>A
XM_017020144.1:c.299-9329C>A	XP_016875633.1:n.299-9329C>A
XR_001748908.1:n.624C>A
XR_001748910.1:n.430-9329C>A
NM_003805.5:c.319C>A MANE Select	NP_003796.1:p.Pro107Thr
NM_001320099.2:c.319C>A	NP_001307028.1:p.Pro107Thr
NM_001320100.2:c.299-44060C>A	NP_001307029.1:n.299-44060C>A
NR_135147.2:n.403-9329C>A