Canonical Allele Identifier: CA481312744
Gene: CRADD HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.94243963G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93850187G>C , CM000674.2:g.93850187G>C GRCh38
NC_000012.11:g.94243963G>C , CM000674.1:g.94243963G>C GRCh37
NC_000012.10:g.92768094G>C NCBI36
NG_032159.1:g.177813G>C
NG_032159.2:g.177813G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000332896.8:c.516G>C MANE Select ENSP00000327647.3:p.Gly172=
ENST00000332896.7:c.516G>C ENSP00000327647.3:p.Gly172=
ENST00000542893.2:c.516G>C ENSP00000439068.2:p.Gly172=
ENST00000548330.1:n.901G>C
ENST00000548483.5:c.299-43863G>C ENSP00000448685.1:n.299-43863G>C
ENST00000550030.1:n.316G>C
ENST00000551065.5:c.299-9132G>C ENSP00000448425.1:n.299-9132G>C
ENST00000609189.1:n.292G>C
NM_003805.3:c.516G>C NP_003796.1:p.Gly172=
XM_005269211.3:c.299-43863G>C XP_005269268.1:n.299-43863G>C
NM_001320099.1:c.516G>C NP_001307028.1:p.Gly172=
NM_001320100.1:c.299-43863G>C NP_001307029.1:n.299-43863G>C
NM_003805.4:c.516G>C NP_003796.1:p.Gly172=
NR_135147.1:n.407-9132G>C
XM_017020144.1:c.299-9132G>C XP_016875633.1:n.299-9132G>C
XR_001748910.1:n.430-9132G>C
NM_003805.5:c.516G>C MANE Select NP_003796.1:p.Gly172=
NM_001320099.2:c.516G>C NP_001307028.1:p.Gly172=
NM_001320100.2:c.299-43863G>C NP_001307029.1:n.299-43863G>C
NR_135147.2:n.403-9132G>C