Canonical Allele Identifier: CA763529110

Gene: CYP20A1

Linked Data

• dbSNP Id: rs1193191740
• gnomAD v3: 2-203300395-T-A
• gnomAD v4: 2-203300395-T-A
• MyVariant Identifiers: chr2:g.204165118T>A (hg19) ; chr2:g.203300395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203300395T>A , CM000664.2:g.203300395T>A	GRCh38
NC_000002.11:g.204165118T>A , CM000664.1:g.204165118T>A	GRCh37
NC_000002.10:g.203873363T>A	NCBI36
NG_007956.1:g.66955T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356079.9:c.*3487T>A MANE Select	ENSP00000348380.4:n.*3487T>A
ENST00000611416.4:c.*3487T>A	ENSP00000477866.1:n.*3487T>A
ENST00000613925.4:c.*380+3107T>A	ENSP00000482757.1:n.*380+3107T>A
NM_177538.2:c.*3487T>A	NP_803882.1:n.*3487T>A
NM_001371695.1:c.*3487T>A	NP_001358624.1:n.*3487T>A
NM_001371696.1:c.*3487T>A	NP_001358625.1:n.*3487T>A
NM_001371697.1:c.*3487T>A	NP_001358626.1:n.*3487T>A
NM_001371698.1:c.*3487T>A	NP_001358627.1:n.*3487T>A
NM_001371699.1:c.*3487T>A	NP_001358628.1:n.*3487T>A
NM_001371700.1:c.*3487T>A	NP_001358629.1:n.*3487T>A
NM_001371701.1:c.*3487T>A	NP_001358630.1:n.*3487T>A
NM_001371702.1:c.*3487T>A	NP_001358631.1:n.*3487T>A
NM_001371703.1:c.*3487T>A	NP_001358632.1:n.*3487T>A
NM_001371704.1:c.*3487T>A	NP_001358633.1:n.*3487T>A
NM_001371705.1:c.*3487T>A	NP_001358634.1:n.*3487T>A
NM_001371706.1:c.*3487T>A	NP_001358635.1:n.*3487T>A
NM_177538.3:c.*3487T>A MANE Select	NP_803882.1:n.*3487T>A
NR_163981.1:n.4800T>A
NR_163982.1:n.4721T>A
NR_163983.1:n.4504T>A
NR_163984.1:n.4563T>A
NR_163985.1:n.4809T>A