Canonical Allele Identifier: CA386142891

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94244030C>G (hg19) ; chr12:g.93850254C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850254C>G , CM000674.2:g.93850254C>G	GRCh38
NC_000012.11:g.94244030C>G , CM000674.1:g.94244030C>G	GRCh37
NC_000012.10:g.92768161C>G	NCBI36
NG_032159.1:g.177880C>G
NG_032159.2:g.177880C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.583C>G MANE Select	ENSP00000327647.3:p.Leu195Val
ENST00000332896.7:c.583C>G	ENSP00000327647.3:p.Leu195Val
ENST00000542893.2:c.583C>G	ENSP00000439068.2:p.Leu195Val
ENST00000548330.1:n.968C>G
ENST00000548483.5:c.299-43796C>G	ENSP00000448685.1:n.299-43796C>G
ENST00000550030.1:n.383C>G
ENST00000551065.5:c.299-9065C>G	ENSP00000448425.1:n.299-9065C>G
ENST00000609189.1:n.359C>G
NM_003805.3:c.583C>G	NP_003796.1:p.Leu195Val
XM_005269211.3:c.299-43796C>G	XP_005269268.1:n.299-43796C>G
NM_001320099.1:c.583C>G	NP_001307028.1:p.Leu195Val
NM_001320100.1:c.299-43796C>G	NP_001307029.1:n.299-43796C>G
NM_003805.4:c.583C>G	NP_003796.1:p.Leu195Val
NR_135147.1:n.407-9065C>G
XM_017020144.1:c.299-9065C>G	XP_016875633.1:n.299-9065C>G
XR_001748910.1:n.430-9065C>G
NM_003805.5:c.583C>G MANE Select	NP_003796.1:p.Leu195Val
NM_001320099.2:c.583C>G	NP_001307028.1:p.Leu195Val
NM_001320100.2:c.299-43796C>G	NP_001307029.1:n.299-43796C>G
NR_135147.2:n.403-9065C>G