Canonical Allele Identifier: CA1321887723

Gene: CYP20A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203300386T= , CM000664.2:g.203300386T=	GRCh38
NC_000002.11:g.204165109T= , CM000664.1:g.204165109T=	GRCh37
NC_000002.10:g.203873354T=	NCBI36
NG_007956.1:g.66946T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356079.9:c.*3478T= MANE Select	ENSP00000348380.4:n.*3478T=
ENST00000611416.4:c.*3478T=	ENSP00000477866.1:n.*3478T=
ENST00000613925.4:c.*380+3098T=	ENSP00000482757.1:n.*380+3098T=
NM_177538.2:c.*3478T=	NP_803882.1:n.*3478T=
NM_001371695.1:c.*3478T=	NP_001358624.1:n.*3478T=
NM_001371696.1:c.*3478T=	NP_001358625.1:n.*3478T=
NM_001371697.1:c.*3478T=	NP_001358626.1:n.*3478T=
NM_001371698.1:c.*3478T=	NP_001358627.1:n.*3478T=
NM_001371699.1:c.*3478T=	NP_001358628.1:n.*3478T=
NM_001371700.1:c.*3478T=	NP_001358629.1:n.*3478T=
NM_001371701.1:c.*3478T=	NP_001358630.1:n.*3478T=
NM_001371702.1:c.*3478T=	NP_001358631.1:n.*3478T=
NM_001371703.1:c.*3478T=	NP_001358632.1:n.*3478T=
NM_001371704.1:c.*3478T=	NP_001358633.1:n.*3478T=
NM_001371705.1:c.*3478T=	NP_001358634.1:n.*3478T=
NM_001371706.1:c.*3478T=	NP_001358635.1:n.*3478T=
NM_177538.3:c.*3478T= MANE Select	NP_803882.1:n.*3478T=
NR_163981.1:n.4791T=
NR_163982.1:n.4712T=
NR_163983.1:n.4495T=
NR_163984.1:n.4554T=
NR_163985.1:n.4800T=