Canonical Allele Identifier: CA2610723991
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834080dup , CM000672.2:g.102834080dup GRCh38
NC_000010.10:g.104593837dup , CM000672.1:g.104593837dup GRCh37
NC_000010.9:g.104583827dup NCBI36
NG_007955.1:g.8457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-97dup
ENST00000369887.4:c.712dup (CYP17A1) MANE Select ENSP00000358903.3:p.Ile238AsnfsTer4
ENST00000638190.1:c.666+708dup (CYP17A1) ENSP00000492539.1:n.666+708dup
ENST00000638272.1:c.298-869dup (CYP17A1) ENSP00000491508.1:n.298-869dup
ENST00000638971.1:c.666+708dup (CYP17A1) ENSP00000492313.1:n.666+708dup
ENST00000639393.1:c.712dup (CYP17A1) ENSP00000492651.1:p.Ile238AsnfsTer4
ENST00000640633.1:n.474dup (CYP17A1)
ENST00000369887.3:c.712dup (CYP17A1) ENSP00000358903.3:p.Ile238AsnfsTer4
ENST00000489268.1:n.1628dup (CYP17A1)
NM_000102.3:c.712dup (CYP17A1) NP_000093.1:p.Ile238AsnfsTer4
XR_428804.1:n.206-97dup (CYP17A1-AS1)
NM_000102.4:c.712dup (CYP17A1) MANE Select NP_000093.1:p.Ile238AsnfsTer4