Canonical Allele Identifier: CA595636716

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• dbSNP Id: rs1489861261
• gnomAD v2: 10-104593752-C-G
• gnomAD v4: 10-102833995-C-G
• MyVariant Identifiers: chr10:g.104593752C>G (hg19) ; chr10:g.102833995C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833995C>G , CM000672.2:g.102833995C>G	GRCh38
NC_000010.10:g.104593752C>G , CM000672.1:g.104593752C>G	GRCh37
NC_000010.9:g.104583742C>G	NCBI36
NG_007955.1:g.8539G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-182C>G
ENST00000369887.4:c.753+41G>C (CYP17A1) MANE Select	ENSP00000358903.3:n.753+41G>C
ENST00000638190.1:c.666+790G>C (CYP17A1)	ENSP00000492539.1:n.666+790G>C
ENST00000638272.1:c.298-787G>C (CYP17A1)	ENSP00000491508.1:n.298-787G>C
ENST00000638971.1:c.667-787G>C (CYP17A1)	ENSP00000492313.1:n.667-787G>C
ENST00000639393.1:c.753+41G>C (CYP17A1)	ENSP00000492651.1:n.753+41G>C
ENST00000640633.1:n.515+41G>C (CYP17A1)
ENST00000369887.3:c.753+41G>C (CYP17A1)	ENSP00000358903.3:n.753+41G>C
ENST00000489268.1:n.1710G>C (CYP17A1)
NM_000102.3:c.753+41G>C (CYP17A1)	NP_000093.1:n.753+41G>C
XR_428804.1:n.206-182C>G (CYP17A1-AS1)
NM_000102.4:c.753+41G>C (CYP17A1) MANE Select	NP_000093.1:n.753+41G>C