Canonical Allele Identifier: CA5669477

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• dbSNP Id: rs763622768
• ExAC: 10:104593760 C / T
• gnomAD v2: 10-104593760-C-T
• gnomAD v4: 10-102834003-C-T
• MyVariant Identifiers: chr10:g.104593760C>T (hg19) ; chr10:g.102834003C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834003C>T , CM000672.2:g.102834003C>T	GRCh38
NC_000010.10:g.104593760C>T , CM000672.1:g.104593760C>T	GRCh37
NC_000010.9:g.104583750C>T	NCBI36
NG_007955.1:g.8531G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-174C>T
ENST00000369887.4:c.753+33G>A (CYP17A1) MANE Select	ENSP00000358903.3:n.753+33G>A
ENST00000638190.1:c.666+782G>A (CYP17A1)	ENSP00000492539.1:n.666+782G>A
ENST00000638272.1:c.298-795G>A (CYP17A1)	ENSP00000491508.1:n.298-795G>A
ENST00000638971.1:c.666+782G>A (CYP17A1)	ENSP00000492313.1:n.666+782G>A
ENST00000639393.1:c.753+33G>A (CYP17A1)	ENSP00000492651.1:n.753+33G>A
ENST00000640633.1:n.515+33G>A (CYP17A1)
ENST00000369887.3:c.753+33G>A (CYP17A1)	ENSP00000358903.3:n.753+33G>A
ENST00000489268.1:n.1702G>A (CYP17A1)
NM_000102.3:c.753+33G>A (CYP17A1)	NP_000093.1:n.753+33G>A
XR_428804.1:n.206-174C>T (CYP17A1-AS1)
NM_000102.4:c.753+33G>A (CYP17A1) MANE Select	NP_000093.1:n.753+33G>A