Canonical Allele Identifier: CA6720218

Gene: CRADD

Linked Data

• ClinVar Variation Id: 1259541
• ClinVar RCV Id: RCV001673917
• dbSNP Id: rs56944668
• ExAC: 12:94243853 C / T
• gnomAD v2: 12-94243853-C-T
• gnomAD v3: 12-93850077-C-T
• gnomAD v4: 12-93850077-C-T
• MyVariant Identifiers: chr12:g.94243853C>T (hg19) ; chr12:g.93850077C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850077C>T , CM000674.2:g.93850077C>T	GRCh38
NC_000012.11:g.94243853C>T , CM000674.1:g.94243853C>T	GRCh37
NC_000012.10:g.92767984C>T	NCBI36
NG_032159.1:g.177703C>T
NG_032159.2:g.177703C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.406C>T MANE Select	ENSP00000327647.3:p.Leu136=
ENST00000332896.7:c.406C>T	ENSP00000327647.3:p.Leu136=
ENST00000542893.2:c.406C>T	ENSP00000439068.2:p.Leu136=
ENST00000548330.1:n.791C>T
ENST00000548483.5:c.299-43973C>T	ENSP00000448685.1:n.299-43973C>T
ENST00000550030.1:n.206C>T
ENST00000551065.5:c.299-9242C>T	ENSP00000448425.1:n.299-9242C>T
ENST00000609189.1:n.182C>T
NM_003805.3:c.406C>T	NP_003796.1:p.Leu136=
XM_005269211.3:c.299-43973C>T	XP_005269268.1:n.299-43973C>T
NM_001320099.1:c.406C>T	NP_001307028.1:p.Leu136=
NM_001320100.1:c.299-43973C>T	NP_001307029.1:n.299-43973C>T
NM_003805.4:c.406C>T	NP_003796.1:p.Leu136=
NR_135147.1:n.407-9242C>T
XM_017020144.1:c.299-9242C>T	XP_016875633.1:n.299-9242C>T
XR_001748910.1:n.430-9242C>T
NM_003805.5:c.406C>T MANE Select	NP_003796.1:p.Leu136=
NM_001320099.2:c.406C>T	NP_001307028.1:p.Leu136=
NM_001320100.2:c.299-43973C>T	NP_001307029.1:n.299-43973C>T
NR_135147.2:n.403-9242C>T