Canonical Allele Identifier: CA212293141

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• dbSNP Id: rs2911432
• gnomAD v4: 10-102833994-A-C
• MyVariant Identifiers: chr10:g.104593751A>C (hg19) ; chr10:g.102833994A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833994A>C , CM000672.2:g.102833994A>C	GRCh38
NC_000010.10:g.104593751A>C , CM000672.1:g.104593751A>C	GRCh37
NC_000010.9:g.104583741A>C	NCBI36
NG_007955.1:g.8540T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-183A>C
ENST00000369887.4:c.753+42T>G (CYP17A1) MANE Select	ENSP00000358903.3:n.753+42T>G
ENST00000638190.1:c.666+791T>G (CYP17A1)	ENSP00000492539.1:n.666+791T>G
ENST00000638272.1:c.298-786T>G (CYP17A1)	ENSP00000491508.1:n.298-786T>G
ENST00000638971.1:c.667-786T>G (CYP17A1)	ENSP00000492313.1:n.667-786T>G
ENST00000639393.1:c.753+42T>G (CYP17A1)	ENSP00000492651.1:n.753+42T>G
ENST00000640633.1:n.515+42T>G (CYP17A1)
ENST00000369887.3:c.753+42T>G (CYP17A1)	ENSP00000358903.3:n.753+42T>G
ENST00000489268.1:n.1711T>G (CYP17A1)
NM_000102.3:c.753+42T>G (CYP17A1)	NP_000093.1:n.753+42T>G
XR_428804.1:n.206-183A>C (CYP17A1-AS1)
NM_000102.4:c.753+42T>G (CYP17A1) MANE Select	NP_000093.1:n.753+42T>G