Canonical Allele Identifier: CA386142678

Gene: CRADD

Linked Data

• dbSNP Id: rs1958197538
• gnomAD v3: 12-93850150-T-C
• gnomAD v4: 12-93850150-T-C
• MyVariant Identifiers: chr12:g.94243926T>C (hg19) ; chr12:g.93850150T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850150T>C , CM000674.2:g.93850150T>C	GRCh38
NC_000012.11:g.94243926T>C , CM000674.1:g.94243926T>C	GRCh37
NC_000012.10:g.92768057T>C	NCBI36
NG_032159.1:g.177776T>C
NG_032159.2:g.177776T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.479T>C MANE Select	ENSP00000327647.3:p.Val160Ala
ENST00000332896.7:c.479T>C	ENSP00000327647.3:p.Val160Ala
ENST00000542893.2:c.479T>C	ENSP00000439068.2:p.Val160Ala
ENST00000548330.1:n.864T>C
ENST00000548483.5:c.299-43900T>C	ENSP00000448685.1:n.299-43900T>C
ENST00000550030.1:n.279T>C
ENST00000551065.5:c.299-9169T>C	ENSP00000448425.1:n.299-9169T>C
ENST00000609189.1:n.255T>C
NM_003805.3:c.479T>C	NP_003796.1:p.Val160Ala
XM_005269211.3:c.299-43900T>C	XP_005269268.1:n.299-43900T>C
NM_001320099.1:c.479T>C	NP_001307028.1:p.Val160Ala
NM_001320100.1:c.299-43900T>C	NP_001307029.1:n.299-43900T>C
NM_003805.4:c.479T>C	NP_003796.1:p.Val160Ala
NR_135147.1:n.407-9169T>C
XM_017020144.1:c.299-9169T>C	XP_016875633.1:n.299-9169T>C
XR_001748910.1:n.430-9169T>C
NM_003805.5:c.479T>C MANE Select	NP_003796.1:p.Val160Ala
NM_001320099.2:c.479T>C	NP_001307028.1:p.Val160Ala
NM_001320100.2:c.299-43900T>C	NP_001307029.1:n.299-43900T>C
NR_135147.2:n.403-9169T>C