Canonical Allele Identifier: CA2055548695

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850103T= , CM000674.2:g.93850103T=	GRCh38
NC_000012.11:g.94243879T= , CM000674.1:g.94243879T=	GRCh37
NC_000012.10:g.92768010T=	NCBI36
NG_032159.1:g.177729T=
NG_032159.2:g.177729T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.432T= MANE Select	ENSP00000327647.3:p.Asp144=
ENST00000332896.7:c.432T=	ENSP00000327647.3:p.Asp144=
ENST00000542893.2:c.432T=	ENSP00000439068.2:p.Asp144=
ENST00000548330.1:n.817T=
ENST00000548483.5:c.299-43947T=	ENSP00000448685.1:n.299-43947T=
ENST00000550030.1:n.232T=
ENST00000551065.5:c.299-9216T=	ENSP00000448425.1:n.299-9216T=
ENST00000609189.1:n.208T=
NM_003805.3:c.432T=	NP_003796.1:p.Asp144=
XM_005269211.3:c.299-43947T=	XP_005269268.1:n.299-43947T=
NM_001320099.1:c.432T=	NP_001307028.1:p.Asp144=
NM_001320100.1:c.299-43947T=	NP_001307029.1:n.299-43947T=
NM_003805.4:c.432T=	NP_003796.1:p.Asp144=
NR_135147.1:n.407-9216T=
XM_017020144.1:c.299-9216T=	XP_016875633.1:n.299-9216T=
XR_001748910.1:n.430-9216T=
NM_003805.5:c.432T= MANE Select	NP_003796.1:p.Asp144=
NM_001320099.2:c.432T=	NP_001307028.1:p.Asp144=
NM_001320100.2:c.299-43947T=	NP_001307029.1:n.299-43947T=
NR_135147.2:n.403-9216T=