Canonical Allele Identifier: CA2620206618

Gene: CRADD

Linked Data

• gnomAD v4: 12-93850290-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850290C>T , CM000674.2:g.93850290C>T	GRCh38
NC_000012.11:g.94244066C>T , CM000674.1:g.94244066C>T	GRCh37
NC_000012.10:g.92768197C>T	NCBI36
NG_032159.1:g.177916C>T
NG_032159.2:g.177916C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.*19C>T MANE Select	ENSP00000327647.3:n.*19C>T
ENST00000332896.7:c.*19C>T	ENSP00000327647.3:n.*19C>T
ENST00000542893.2:c.*19C>T	ENSP00000439068.2:n.*19C>T
ENST00000548330.1:n.1004C>T
ENST00000548483.5:c.299-43760C>T	ENSP00000448685.1:n.299-43760C>T
ENST00000550030.1:n.419C>T
ENST00000551065.5:c.299-9029C>T	ENSP00000448425.1:n.299-9029C>T
ENST00000609189.1:n.395C>T
NM_003805.3:c.*19C>T	NP_003796.1:n.*19C>T
XM_005269211.3:c.299-43760C>T	XP_005269268.1:n.299-43760C>T
NM_001320099.1:c.*19C>T	NP_001307028.1:n.*19C>T
NM_001320100.1:c.299-43760C>T	NP_001307029.1:n.299-43760C>T
NM_003805.4:c.*19C>T	NP_003796.1:n.*19C>T
NR_135147.1:n.407-9029C>T
XM_017020144.1:c.299-9029C>T	XP_016875633.1:n.299-9029C>T
XR_001748910.1:n.430-9029C>T
NM_003805.5:c.*19C>T MANE Select	NP_003796.1:n.*19C>T
NM_001320099.2:c.*19C>T	NP_001307028.1:n.*19C>T
NM_001320100.2:c.299-43760C>T	NP_001307029.1:n.299-43760C>T
NR_135147.2:n.403-9029C>T