Canonical Allele Identifier: CA386142417

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243804G>C (hg19) ; chr12:g.93850028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850028G>C , CM000674.2:g.93850028G>C	GRCh38
NC_000012.11:g.94243804G>C , CM000674.1:g.94243804G>C	GRCh37
NC_000012.10:g.92767935G>C	NCBI36
NG_032159.1:g.177654G>C
NG_032159.2:g.177654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.357G>C MANE Select	ENSP00000327647.3:p.Gln119His
ENST00000332896.7:c.357G>C	ENSP00000327647.3:p.Gln119His
ENST00000542893.2:c.357G>C	ENSP00000439068.2:p.Gln119His
ENST00000548330.1:n.742G>C
ENST00000548483.5:c.299-44022G>C	ENSP00000448685.1:n.299-44022G>C
ENST00000550030.1:n.157G>C
ENST00000551065.5:c.299-9291G>C	ENSP00000448425.1:n.299-9291G>C
ENST00000609189.1:n.133G>C
NM_003805.3:c.357G>C	NP_003796.1:p.Gln119His
XM_005269211.3:c.299-44022G>C	XP_005269268.1:n.299-44022G>C
NM_001320099.1:c.357G>C	NP_001307028.1:p.Gln119His
NM_001320100.1:c.299-44022G>C	NP_001307029.1:n.299-44022G>C
NM_003805.4:c.357G>C	NP_003796.1:p.Gln119His
NR_135147.1:n.407-9291G>C
XM_017020144.1:c.299-9291G>C	XP_016875633.1:n.299-9291G>C
XR_001748910.1:n.430-9291G>C
NM_003805.5:c.357G>C MANE Select	NP_003796.1:p.Gln119His
NM_001320099.2:c.357G>C	NP_001307028.1:p.Gln119His
NM_001320100.2:c.299-44022G>C	NP_001307029.1:n.299-44022G>C
NR_135147.2:n.403-9291G>C