Canonical Allele Identifier: CA386142701

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243938T>A (hg19) ; chr12:g.93850162T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850162T>A , CM000674.2:g.93850162T>A	GRCh38
NC_000012.11:g.94243938T>A , CM000674.1:g.94243938T>A	GRCh37
NC_000012.10:g.92768069T>A	NCBI36
NG_032159.1:g.177788T>A
NG_032159.2:g.177788T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.491T>A MANE Select	ENSP00000327647.3:p.Phe164Tyr
ENST00000332896.7:c.491T>A	ENSP00000327647.3:p.Phe164Tyr
ENST00000542893.2:c.491T>A	ENSP00000439068.2:p.Phe164Tyr
ENST00000548330.1:n.876T>A
ENST00000548483.5:c.299-43888T>A	ENSP00000448685.1:n.299-43888T>A
ENST00000550030.1:n.291T>A
ENST00000551065.5:c.299-9157T>A	ENSP00000448425.1:n.299-9157T>A
ENST00000609189.1:n.267T>A
NM_003805.3:c.491T>A	NP_003796.1:p.Phe164Tyr
XM_005269211.3:c.299-43888T>A	XP_005269268.1:n.299-43888T>A
NM_001320099.1:c.491T>A	NP_001307028.1:p.Phe164Tyr
NM_001320100.1:c.299-43888T>A	NP_001307029.1:n.299-43888T>A
NM_003805.4:c.491T>A	NP_003796.1:p.Phe164Tyr
NR_135147.1:n.407-9157T>A
XM_017020144.1:c.299-9157T>A	XP_016875633.1:n.299-9157T>A
XR_001748910.1:n.430-9157T>A
NM_003805.5:c.491T>A MANE Select	NP_003796.1:p.Phe164Tyr
NM_001320099.2:c.491T>A	NP_001307028.1:p.Phe164Tyr
NM_001320100.2:c.299-43888T>A	NP_001307029.1:n.299-43888T>A
NR_135147.2:n.403-9157T>A