Canonical Allele Identifier: CA386142912

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94244039T>A (hg19) ; chr12:g.93850263T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850263T>A , CM000674.2:g.93850263T>A	GRCh38
NC_000012.11:g.94244039T>A , CM000674.1:g.94244039T>A	GRCh37
NC_000012.10:g.92768170T>A	NCBI36
NG_032159.1:g.177889T>A
NG_032159.2:g.177889T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.592T>A MANE Select	ENSP00000327647.3:p.Leu198Met
ENST00000332896.7:c.592T>A	ENSP00000327647.3:p.Leu198Met
ENST00000542893.2:c.592T>A	ENSP00000439068.2:p.Leu198Met
ENST00000548330.1:n.977T>A
ENST00000548483.5:c.299-43787T>A	ENSP00000448685.1:n.299-43787T>A
ENST00000550030.1:n.392T>A
ENST00000551065.5:c.299-9056T>A	ENSP00000448425.1:n.299-9056T>A
ENST00000609189.1:n.368T>A
NM_003805.3:c.592T>A	NP_003796.1:p.Leu198Met
XM_005269211.3:c.299-43787T>A	XP_005269268.1:n.299-43787T>A
NM_001320099.1:c.592T>A	NP_001307028.1:p.Leu198Met
NM_001320100.1:c.299-43787T>A	NP_001307029.1:n.299-43787T>A
NM_003805.4:c.592T>A	NP_003796.1:p.Leu198Met
NR_135147.1:n.407-9056T>A
XM_017020144.1:c.299-9056T>A	XP_016875633.1:n.299-9056T>A
XR_001748910.1:n.430-9056T>A
NM_003805.5:c.592T>A MANE Select	NP_003796.1:p.Leu198Met
NM_001320099.2:c.592T>A	NP_001307028.1:p.Leu198Met
NM_001320100.2:c.299-43787T>A	NP_001307029.1:n.299-43787T>A
NR_135147.2:n.403-9056T>A