Canonical Allele Identifier: CA6720253
Gene: CRADD HGNC NCBI

Linked Data

dbSNP Id: rs760877938

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93850207G>A , CM000674.2:g.93850207G>A GRCh38
NC_000012.11:g.94243983G>A , CM000674.1:g.94243983G>A GRCh37
NC_000012.10:g.92768114G>A NCBI36
NG_032159.1:g.177833G>A
NG_032159.2:g.177833G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332896.8:c.536G>A MANE Select ENSP00000327647.3:p.Ser179Asn
ENST00000332896.7:c.536G>A ENSP00000327647.3:p.Ser179Asn
ENST00000542893.2:c.536G>A ENSP00000439068.2:p.Ser179Asn
ENST00000548330.1:n.921G>A
ENST00000548483.5:c.299-43843G>A ENSP00000448685.1:n.299-43843G>A
ENST00000550030.1:n.336G>A
ENST00000551065.5:c.299-9112G>A ENSP00000448425.1:n.299-9112G>A
ENST00000609189.1:n.312G>A
NM_003805.3:c.536G>A NP_003796.1:p.Ser179Asn
XM_005269211.3:c.299-43843G>A XP_005269268.1:n.299-43843G>A
NM_001320099.1:c.536G>A NP_001307028.1:p.Ser179Asn
NM_001320100.1:c.299-43843G>A NP_001307029.1:n.299-43843G>A
NM_003805.4:c.536G>A NP_003796.1:p.Ser179Asn
NR_135147.1:n.407-9112G>A
XM_017020144.1:c.299-9112G>A XP_016875633.1:n.299-9112G>A
XR_001748910.1:n.430-9112G>A
NM_003805.5:c.536G>A MANE Select NP_003796.1:p.Ser179Asn
NM_001320099.2:c.536G>A NP_001307028.1:p.Ser179Asn
NM_001320100.2:c.299-43843G>A NP_001307029.1:n.299-43843G>A
NR_135147.2:n.403-9112G>A