Canonical Allele Identifier: CA2055549045

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850291T= , CM000674.2:g.93850291T=	GRCh38
NC_000012.11:g.94244067T= , CM000674.1:g.94244067T=	GRCh37
NC_000012.10:g.92768198T=	NCBI36
NG_032159.1:g.177917T=
NG_032159.2:g.177917T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.*20T= MANE Select	ENSP00000327647.3:n.*20T=
ENST00000332896.7:c.*20T=	ENSP00000327647.3:n.*20T=
ENST00000542893.2:c.*20T=	ENSP00000439068.2:n.*20T=
ENST00000548330.1:n.1005T=
ENST00000548483.5:c.299-43759T=	ENSP00000448685.1:n.299-43759T=
ENST00000550030.1:n.420T=
ENST00000551065.5:c.299-9028T=	ENSP00000448425.1:n.299-9028T=
ENST00000609189.1:n.396T=
NM_003805.3:c.*20T=	NP_003796.1:n.*20T=
XM_005269211.3:c.299-43759T=	XP_005269268.1:n.299-43759T=
NM_001320099.1:c.*20T=	NP_001307028.1:n.*20T=
NM_001320100.1:c.299-43759T=	NP_001307029.1:n.299-43759T=
NM_003805.4:c.*20T=	NP_003796.1:n.*20T=
NR_135147.1:n.407-9028T=
XM_017020144.1:c.299-9028T=	XP_016875633.1:n.299-9028T=
XR_001748910.1:n.430-9028T=
NM_003805.5:c.*20T= MANE Select	NP_003796.1:n.*20T=
NM_001320099.2:c.*20T=	NP_001307028.1:n.*20T=
NM_001320100.2:c.299-43759T=	NP_001307029.1:n.299-43759T=
NR_135147.2:n.403-9028T=