Canonical Allele Identifier: CA386142401

Gene: CRADD

Linked Data

• gnomAD v4: 12-93850020-G-A
• MyVariant Identifiers: chr12:g.94243796G>A (hg19) ; chr12:g.93850020G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850020G>A , CM000674.2:g.93850020G>A	GRCh38
NC_000012.11:g.94243796G>A , CM000674.1:g.94243796G>A	GRCh37
NC_000012.10:g.92767927G>A	NCBI36
NG_032159.1:g.177646G>A
NG_032159.2:g.177646G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.349G>A MANE Select	ENSP00000327647.3:p.Asp117Asn
ENST00000332896.7:c.349G>A	ENSP00000327647.3:p.Asp117Asn
ENST00000542893.2:c.349G>A	ENSP00000439068.2:p.Asp117Asn
ENST00000548330.1:n.734G>A
ENST00000548483.5:c.299-44030G>A	ENSP00000448685.1:n.299-44030G>A
ENST00000550030.1:n.149G>A
ENST00000551065.5:c.299-9299G>A	ENSP00000448425.1:n.299-9299G>A
ENST00000609189.1:n.125G>A
NM_003805.3:c.349G>A	NP_003796.1:p.Asp117Asn
XM_005269211.3:c.299-44030G>A	XP_005269268.1:n.299-44030G>A
NM_001320099.1:c.349G>A	NP_001307028.1:p.Asp117Asn
NM_001320100.1:c.299-44030G>A	NP_001307029.1:n.299-44030G>A
NM_003805.4:c.349G>A	NP_003796.1:p.Asp117Asn
NR_135147.1:n.407-9299G>A
XM_017020144.1:c.299-9299G>A	XP_016875633.1:n.299-9299G>A
XR_001748908.1:n.654G>A
XR_001748910.1:n.430-9299G>A
NM_003805.5:c.349G>A MANE Select	NP_003796.1:p.Asp117Asn
NM_001320099.2:c.349G>A	NP_001307028.1:p.Asp117Asn
NM_001320100.2:c.299-44030G>A	NP_001307029.1:n.299-44030G>A
NR_135147.2:n.403-9299G>A