Canonical Allele Identifier: CA659058231

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs1465326958
• gnomAD v4: 10-102833829-T-C
• MyVariant Identifiers: chr10:g.104593586T>C (hg19) ; chr10:g.102833829T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833829T>C , CM000672.2:g.102833829T>C	GRCh38
NC_000010.10:g.104593586T>C , CM000672.1:g.104593586T>C	GRCh37
NC_000010.9:g.104583576T>C	NCBI36
NG_007955.1:g.8705A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-348T>C
ENST00000369887.4:c.753+207A>G (CYP17A1) MANE Select	ENSP00000358903.3:n.753+207A>G
ENST00000638190.1:c.666+956A>G (CYP17A1)	ENSP00000492539.1:n.666+956A>G
ENST00000638272.1:c.298-621A>G (CYP17A1)	ENSP00000491508.1:n.298-621A>G
ENST00000638971.1:c.667-621A>G (CYP17A1)	ENSP00000492313.1:n.667-621A>G
ENST00000639393.1:c.753+207A>G (CYP17A1)	ENSP00000492651.1:n.753+207A>G
ENST00000640633.1:n.515+207A>G (CYP17A1)
ENST00000647664.1:c.*2860T>C (WBP1L)	ENSP00000498131.1:n.*2860T>C
ENST00000369887.3:c.753+207A>G (CYP17A1)	ENSP00000358903.3:n.753+207A>G
ENST00000489268.1:n.1876A>G (CYP17A1)
NM_000102.3:c.753+207A>G (CYP17A1)	NP_000093.1:n.753+207A>G
XR_428804.1:n.206-348T>C (CYP17A1-AS1)
NM_000102.4:c.753+207A>G (CYP17A1) MANE Select	NP_000093.1:n.753+207A>G