Canonical Allele Identifier: CA659056965

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1350059914
• MyVariant Identifiers: chr10:g.104592243G>C (hg19) ; chr10:g.102832486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832486G>C , CM000672.2:g.102832486G>C	GRCh38
NC_000010.10:g.104592243G>C , CM000672.1:g.104592243G>C	GRCh37
NC_000010.9:g.104582233G>C	NCBI36
NG_007955.1:g.10048C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1139+25C>G (CYP17A1) MANE Select	ENSP00000358903.3:n.1139+25C>G
ENST00000638190.1:c.836+25C>G (CYP17A1)	ENSP00000492539.1:n.836+25C>G
ENST00000638272.1:c.683+25C>G (CYP17A1)	ENSP00000491508.1:n.683+25C>G
ENST00000638971.1:c.1052+25C>G (CYP17A1)	ENSP00000492313.1:n.1052+25C>G
ENST00000639393.1:c.1139+25C>G (CYP17A1)	ENSP00000492651.1:n.1139+25C>G
ENST00000640633.1:n.901+25C>G (CYP17A1)
ENST00000647664.1:c.*1517G>C (WBP1L)	ENSP00000498131.1:n.*1517G>C
ENST00000369887.3:c.1139+25C>G (CYP17A1)	ENSP00000358903.3:n.1139+25C>G
NM_000102.3:c.1139+25C>G (CYP17A1)	NP_000093.1:n.1139+25C>G
NM_000102.4:c.1139+25C>G (CYP17A1) MANE Select	NP_000093.1:n.1139+25C>G