Canonical Allele Identifier: CA386142756

Gene: CRADD

Linked Data

• MyVariant Identifiers: chr12:g.94243965A>T (hg19) ; chr12:g.93850189A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93850189A>T , CM000674.2:g.93850189A>T	GRCh38
NC_000012.11:g.94243965A>T , CM000674.1:g.94243965A>T	GRCh37
NC_000012.10:g.92768096A>T	NCBI36
NG_032159.1:g.177815A>T
NG_032159.2:g.177815A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332896.8:c.518A>T MANE Select	ENSP00000327647.3:p.Lys173Met
ENST00000332896.7:c.518A>T	ENSP00000327647.3:p.Lys173Met
ENST00000542893.2:c.518A>T	ENSP00000439068.2:p.Lys173Met
ENST00000548330.1:n.903A>T
ENST00000548483.5:c.299-43861A>T	ENSP00000448685.1:n.299-43861A>T
ENST00000550030.1:n.318A>T
ENST00000551065.5:c.299-9130A>T	ENSP00000448425.1:n.299-9130A>T
ENST00000609189.1:n.294A>T
NM_003805.3:c.518A>T	NP_003796.1:p.Lys173Met
XM_005269211.3:c.299-43861A>T	XP_005269268.1:n.299-43861A>T
NM_001320099.1:c.518A>T	NP_001307028.1:p.Lys173Met
NM_001320100.1:c.299-43861A>T	NP_001307029.1:n.299-43861A>T
NM_003805.4:c.518A>T	NP_003796.1:p.Lys173Met
NR_135147.1:n.407-9130A>T
XM_017020144.1:c.299-9130A>T	XP_016875633.1:n.299-9130A>T
XR_001748910.1:n.430-9130A>T
NM_003805.5:c.518A>T MANE Select	NP_003796.1:p.Lys173Met
NM_001320099.2:c.518A>T	NP_001307028.1:p.Lys173Met
NM_001320100.2:c.299-43861A>T	NP_001307029.1:n.299-43861A>T
NR_135147.2:n.403-9130A>T