Canonical Allele Identifier: CA481312665

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243927G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850151G>C , CM000674.2:g.93850151G>C	GRCh38
NC_000012.11:g.94243927G>C , CM000674.1:g.94243927G>C	GRCh37
NC_000012.10:g.92768058G>C	NCBI36
NG_032159.1:g.177777G>C
NG_032159.2:g.177777G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.480G>C MANE Select	ENSP00000327647.3:p.Val160=
ENST00000332896.7:c.480G>C	ENSP00000327647.3:p.Val160=
ENST00000542893.2:c.480G>C	ENSP00000439068.2:p.Val160=
ENST00000548330.1:n.865G>C
ENST00000548483.5:c.299-43899G>C	ENSP00000448685.1:n.299-43899G>C
ENST00000550030.1:n.280G>C
ENST00000551065.5:c.299-9168G>C	ENSP00000448425.1:n.299-9168G>C
ENST00000609189.1:n.256G>C
NM_003805.3:c.480G>C	NP_003796.1:p.Val160=
XM_005269211.3:c.299-43899G>C	XP_005269268.1:n.299-43899G>C
NM_001320099.1:c.480G>C	NP_001307028.1:p.Val160=
NM_001320100.1:c.299-43899G>C	NP_001307029.1:n.299-43899G>C
NM_003805.4:c.480G>C	NP_003796.1:p.Val160=
NR_135147.1:n.407-9168G>C
XM_017020144.1:c.299-9168G>C	XP_016875633.1:n.299-9168G>C
XR_001748910.1:n.430-9168G>C
NM_003805.5:c.480G>C MANE Select	NP_003796.1:p.Val160=
NM_001320099.2:c.480G>C	NP_001307028.1:p.Val160=
NM_001320100.2:c.299-43899G>C	NP_001307029.1:n.299-43899G>C
NR_135147.2:n.403-9168G>C