Canonical Allele Identifier: CA386142537

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243859C>G (hg19) ; chr12:g.93850083C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850083C>G , CM000674.2:g.93850083C>G	GRCh38
NC_000012.11:g.94243859C>G , CM000674.1:g.94243859C>G	GRCh37
NC_000012.10:g.92767990C>G	NCBI36
NG_032159.1:g.177709C>G
NG_032159.2:g.177709C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332896.8:c.412C>G MANE Select	ENSP00000327647.3:p.Leu138Val
ENST00000332896.7:c.412C>G	ENSP00000327647.3:p.Leu138Val
ENST00000542893.2:c.412C>G	ENSP00000439068.2:p.Leu138Val
ENST00000548330.1:n.797C>G
ENST00000548483.5:c.299-43967C>G	ENSP00000448685.1:n.299-43967C>G
ENST00000550030.1:n.212C>G
ENST00000551065.5:c.299-9236C>G	ENSP00000448425.1:n.299-9236C>G
ENST00000609189.1:n.188C>G
NM_003805.3:c.412C>G	NP_003796.1:p.Leu138Val
XM_005269211.3:c.299-43967C>G	XP_005269268.1:n.299-43967C>G
NM_001320099.1:c.412C>G	NP_001307028.1:p.Leu138Val
NM_001320100.1:c.299-43967C>G	NP_001307029.1:n.299-43967C>G
NM_003805.4:c.412C>G	NP_003796.1:p.Leu138Val
NR_135147.1:n.407-9236C>G
XM_017020144.1:c.299-9236C>G	XP_016875633.1:n.299-9236C>G
XR_001748910.1:n.430-9236C>G
NM_003805.5:c.412C>G MANE Select	NP_003796.1:p.Leu138Val
NM_001320099.2:c.412C>G	NP_001307028.1:p.Leu138Val
NM_001320100.2:c.299-43967C>G	NP_001307029.1:n.299-43967C>G
NR_135147.2:n.403-9236C>G