Canonical Allele Identifier: CA6720197

Gene: CRADD

Linked Data

• dbSNP Id: rs781157705
• ExAC: 12:94243754 TTGAC / T
• gnomAD v2: 12-94243754-TTGAC-T
• gnomAD v4: 12-93849978-TTGAC-T
• MyVariant Identifiers: chr12:g.94243755_94243758del (hg19) ; chr12:g.93849979_93849982del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93849981_93849984del , CM000674.2:g.93849981_93849984del	GRCh38
NC_000012.11:g.94243757_94243760del , CM000674.1:g.94243757_94243760del	GRCh37
NC_000012.10:g.92767888_92767891del	NCBI36
NG_032159.1:g.177607_177610del
NG_032159.2:g.177607_177610del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.310_313del MANE Select	ENSP00000327647.3:p.Thr104GlyfsTer?
ENST00000332896.7:c.310_313del	ENSP00000327647.3:p.Thr104GlyfsTer?
ENST00000542893.2:c.310_313del	ENSP00000439068.2:p.Thr104GlyfsTer?
ENST00000548330.1:n.695_698del
ENST00000548483.5:c.299-44069_299-44066del	ENSP00000448685.1:n.299-44069_299-44066del
ENST00000550030.1:n.110_113del
ENST00000551065.5:c.299-9338_299-9335del	ENSP00000448425.1:n.299-9338_299-9335del
ENST00000609189.1:n.86_89del
NM_003805.3:c.310_313del	NP_003796.1:p.Thr104GlyfsTer?
XM_005269211.3:c.299-44069_299-44066del	XP_005269268.1:n.299-44069_299-44066del
NM_001320099.1:c.310_313del	NP_001307028.1:p.Thr104GlyfsTer?
NM_001320100.1:c.299-44069_299-44066del	NP_001307029.1:n.299-44069_299-44066del
NM_003805.4:c.310_313del	NP_003796.1:p.Thr104GlyfsTer?
NR_135147.1:n.407-9338_407-9335del
XM_017020144.1:c.299-9338_299-9335del	XP_016875633.1:n.299-9338_299-9335del
XR_001748908.1:n.615_618del
XR_001748909.1:n.611_614del
XR_001748910.1:n.430-9338_430-9335del
NM_003805.5:c.310_313del MANE Select	NP_003796.1:p.Thr104GlyfsTer?
NM_001320099.2:c.310_313del	NP_001307028.1:p.Thr104GlyfsTer?
NM_001320100.2:c.299-44069_299-44066del	NP_001307029.1:n.299-44069_299-44066del
NR_135147.2:n.403-9338_403-9335del