Canonical Allele Identifier: CA1542326846

Gene: CCDC152 SELENOP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42800706C= , CM000667.2:g.42800706C=	GRCh38
NC_000005.9:g.42800808C= , CM000667.1:g.42800808C=	GRCh37
NC_000005.8:g.42836565C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361970.10:c.*925C= (CCDC152) MANE Select	ENSP00000354888.5:n.*925C=
ENST00000514985.6:c.*14G= (SELENOP) MANE Select	ENSP00000420939.1:n.*14G=
ENST00000361970.9:c.*925C= (CCDC152)	ENSP00000354888.5:n.*925C=
ENST00000506577.5:c.*14G= (SELENOP)	ENSP00000425915.1:n.*14G=
ENST00000511224.5:c.*14G= (SELENOP)	ENSP00000427671.1:n.*14G=
ENST00000512980.5:n.3352G= (SELENOP)
ENST00000514985.5:c.*14G= (SELENOP)	ENSP00000420939.1:n.*14G=
NM_001085486.1:c.*14G= (SELENOP)	NP_001078955.1:n.*14G=
NM_001093726.1:c.*14G= (SELENOP)	NP_001087195.1:n.*14G=
NM_001134848.1:c.*925C= (CCDC152)	NP_001128320.1:n.*925C=
NM_005410.2:c.*14G= (SELENOP)	NP_005401.3:n.*14G=
NM_001085486.2:c.*14G= (SELENOP)	NP_001078955.1:n.*14G=
NM_001093726.2:c.*14G= (SELENOP)	NP_001087195.1:n.*14G=
NM_005410.3:c.*14G= (SELENOP)	NP_005401.3:n.*14G=
NM_001134848.2:c.*925C= (CCDC152) MANE Select	NP_001128320.1:n.*925C=
NM_005410.4:c.*14G= (SELENOP) MANE Select	NP_005401.3:n.*14G=
NM_001085486.3:c.*14G= (SELENOP)	NP_001078955.1:n.*14G=
NM_001093726.3:c.*14G= (SELENOP)	NP_001087195.1:n.*14G=