Canonical Allele Identifier: CA2055548457

Gene: CRADD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93849953G= , CM000674.2:g.93849953G=	GRCh38
NC_000012.11:g.94243729G= , CM000674.1:g.94243729G=	GRCh37
NC_000012.10:g.92767860G=	NCBI36
NG_032159.1:g.177579G=
NG_032159.2:g.177579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.299-17G= MANE Select	ENSP00000327647.3:n.299-17G=
ENST00000332896.7:c.299-17G=	ENSP00000327647.3:n.299-17G=
ENST00000542893.2:c.299-17G=	ENSP00000439068.2:n.299-17G=
ENST00000548330.1:n.684-17G=
ENST00000548483.5:c.299-44097G=	ENSP00000448685.1:n.299-44097G=
ENST00000550030.1:n.99-17G=
ENST00000551065.5:c.299-9366G=	ENSP00000448425.1:n.299-9366G=
ENST00000609189.1:n.75-17G=
NM_003805.3:c.299-17G=	NP_003796.1:n.299-17G=
XM_005269211.3:c.299-44097G=	XP_005269268.1:n.299-44097G=
NM_001320099.1:c.299-17G=	NP_001307028.1:n.299-17G=
NM_001320100.1:c.299-44097G=	NP_001307029.1:n.299-44097G=
NM_003805.4:c.299-17G=	NP_003796.1:n.299-17G=
NR_135147.1:n.407-9366G=
XM_017020144.1:c.299-9366G=	XP_016875633.1:n.299-9366G=
XR_001748908.1:n.604-17G=
XR_001748909.1:n.600-17G=
XR_001748910.1:n.430-9366G=
NM_003805.5:c.299-17G= MANE Select	NP_003796.1:n.299-17G=
NM_001320099.2:c.299-17G=	NP_001307028.1:n.299-17G=
NM_001320100.2:c.299-44097G=	NP_001307029.1:n.299-44097G=
NR_135147.2:n.403-9366G=