Canonical Allele Identifier: CA693619772

Gene: CRADD

Linked Data

• dbSNP Id: rs1388946499
• gnomAD v4: 12-93850291-TG-T
• MyVariant Identifiers: chr12:g.94244068del (hg19) ; chr12:g.93850292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850295del , CM000674.2:g.93850295del	GRCh38
NC_000012.11:g.94244071del , CM000674.1:g.94244071del	GRCh37
NC_000012.10:g.92768202del	NCBI36
NG_032159.1:g.177921del
NG_032159.2:g.177921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.*24del MANE Select	ENSP00000327647.3:n.*24del
ENST00000332896.7:c.*24del	ENSP00000327647.3:n.*24del
ENST00000542893.2:c.*24del	ENSP00000439068.2:n.*24del
ENST00000548330.1:n.1009del
ENST00000548483.5:c.299-43755del	ENSP00000448685.1:n.299-43755del
ENST00000550030.1:n.424del
ENST00000551065.5:c.299-9024del	ENSP00000448425.1:n.299-9024del
ENST00000609189.1:n.400del
NM_003805.3:c.*24del	NP_003796.1:n.*24del
XM_005269211.3:c.299-43755del	XP_005269268.1:n.299-43755del
NM_001320099.1:c.*24del	NP_001307028.1:n.*24del
NM_001320100.1:c.299-43755del	NP_001307029.1:n.299-43755del
NM_003805.4:c.*24del	NP_003796.1:n.*24del
NR_135147.1:n.407-9024del
XM_017020144.1:c.299-9024del	XP_016875633.1:n.299-9024del
XR_001748910.1:n.430-9024del
NM_003805.5:c.*24del MANE Select	NP_003796.1:n.*24del
NM_001320099.2:c.*24del	NP_001307028.1:n.*24del
NM_001320100.2:c.299-43755del	NP_001307029.1:n.299-43755del
NR_135147.2:n.403-9024del