Canonical Allele Identifier: CA2055548906

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850198C= , CM000674.2:g.93850198C=	GRCh38
NC_000012.11:g.94243974C= , CM000674.1:g.94243974C=	GRCh37
NC_000012.10:g.92768105C=	NCBI36
NG_032159.1:g.177824C=
NG_032159.2:g.177824C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.527C= MANE Select	ENSP00000327647.3:p.Thr176=
ENST00000332896.7:c.527C=	ENSP00000327647.3:p.Thr176=
ENST00000542893.2:c.527C=	ENSP00000439068.2:p.Thr176=
ENST00000548330.1:n.912C=
ENST00000548483.5:c.299-43852C=	ENSP00000448685.1:n.299-43852C=
ENST00000550030.1:n.327C=
ENST00000551065.5:c.299-9121C=	ENSP00000448425.1:n.299-9121C=
ENST00000609189.1:n.303C=
NM_003805.3:c.527C=	NP_003796.1:p.Thr176=
XM_005269211.3:c.299-43852C=	XP_005269268.1:n.299-43852C=
NM_001320099.1:c.527C=	NP_001307028.1:p.Thr176=
NM_001320100.1:c.299-43852C=	NP_001307029.1:n.299-43852C=
NM_003805.4:c.527C=	NP_003796.1:p.Thr176=
NR_135147.1:n.407-9121C=
XM_017020144.1:c.299-9121C=	XP_016875633.1:n.299-9121C=
XR_001748910.1:n.430-9121C=
NM_003805.5:c.527C= MANE Select	NP_003796.1:p.Thr176=
NM_001320099.2:c.527C=	NP_001307028.1:p.Thr176=
NM_001320100.2:c.299-43852C=	NP_001307029.1:n.299-43852C=
NR_135147.2:n.403-9121C=