Canonical Allele Identifier: CA2610723961

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• dbSNP Id: rs2134083273
• gnomAD v4: 10-102834008-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834008T>A , CM000672.2:g.102834008T>A	GRCh38
NC_000010.10:g.104593765T>A , CM000672.1:g.104593765T>A	GRCh37
NC_000010.9:g.104583755T>A	NCBI36
NG_007955.1:g.8526A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-169T>A
ENST00000369887.4:c.753+28A>T (CYP17A1) MANE Select	ENSP00000358903.3:n.753+28A>T
ENST00000638190.1:c.666+777A>T (CYP17A1)	ENSP00000492539.1:n.666+777A>T
ENST00000638272.1:c.298-800A>T (CYP17A1)	ENSP00000491508.1:n.298-800A>T
ENST00000638971.1:c.666+777A>T (CYP17A1)	ENSP00000492313.1:n.666+777A>T
ENST00000639393.1:c.753+28A>T (CYP17A1)	ENSP00000492651.1:n.753+28A>T
ENST00000640633.1:n.515+28A>T (CYP17A1)
ENST00000369887.3:c.753+28A>T (CYP17A1)	ENSP00000358903.3:n.753+28A>T
ENST00000489268.1:n.1697A>T (CYP17A1)
NM_000102.3:c.753+28A>T (CYP17A1)	NP_000093.1:n.753+28A>T
XR_428804.1:n.206-169T>A (CYP17A1-AS1)
NM_000102.4:c.753+28A>T (CYP17A1) MANE Select	NP_000093.1:n.753+28A>T