Canonical Allele Identifier: CA595226345

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• dbSNP Id: rs1259560771
• gnomAD v2: 10-104593395-T-C
• gnomAD v3: 10-102833638-T-C
• gnomAD v4: 10-102833638-T-C
• MyVariant Identifiers: chr10:g.104593395T>C (hg19) ; chr10:g.102833638T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833638T>C , CM000672.2:g.102833638T>C	GRCh38
NC_000010.10:g.104593395T>C , CM000672.1:g.104593395T>C	GRCh37
NC_000010.9:g.104583385T>C	NCBI36
NG_007955.1:g.8896A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-539T>C
ENST00000369887.4:c.753+398A>G (CYP17A1) MANE Select	ENSP00000358903.3:n.753+398A>G
ENST00000638190.1:c.667-958A>G (CYP17A1)	ENSP00000492539.1:n.667-958A>G
ENST00000638272.1:c.298-430A>G (CYP17A1)	ENSP00000491508.1:n.298-430A>G
ENST00000638971.1:c.667-430A>G (CYP17A1)	ENSP00000492313.1:n.667-430A>G
ENST00000639393.1:c.753+398A>G (CYP17A1)	ENSP00000492651.1:n.753+398A>G
ENST00000640633.1:n.515+398A>G (CYP17A1)
ENST00000647664.1:c.*2669T>C (WBP1L)	ENSP00000498131.1:n.*2669T>C
ENST00000369887.3:c.753+398A>G (CYP17A1)	ENSP00000358903.3:n.753+398A>G
ENST00000489268.1:n.2067A>G (CYP17A1)
NM_000102.3:c.753+398A>G (CYP17A1)	NP_000093.1:n.753+398A>G
XR_428804.1:n.206-539T>C (CYP17A1-AS1)
NM_000102.4:c.753+398A>G (CYP17A1) MANE Select	NP_000093.1:n.753+398A>G