Canonical Allele Identifier: CA377938930

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104592402A>C (hg19) ; chr10:g.102832645A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832645A>C , CM000672.2:g.102832645A>C	GRCh38
NC_000010.10:g.104592402A>C , CM000672.1:g.104592402A>C	GRCh37
NC_000010.9:g.104582392A>C	NCBI36
NG_007955.1:g.9889T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1005T>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Asn335Lys
ENST00000638190.1:c.702T>G (CYP17A1)	ENSP00000492539.1:p.Asn234Lys
ENST00000638272.1:c.549T>G (CYP17A1)	ENSP00000491508.1:p.Asn183Lys
ENST00000638971.1:c.918T>G (CYP17A1)	ENSP00000492313.1:p.Asn306Lys
ENST00000639393.1:c.1005T>G (CYP17A1)	ENSP00000492651.1:p.Asn335Lys
ENST00000640633.1:n.767T>G (CYP17A1)
ENST00000647664.1:c.*1676A>C (WBP1L)	ENSP00000498131.1:n.*1676A>C
ENST00000369887.3:c.1005T>G (CYP17A1)	ENSP00000358903.3:p.Asn335Lys
NM_000102.3:c.1005T>G (CYP17A1)	NP_000093.1:p.Asn335Lys
NM_000102.4:c.1005T>G (CYP17A1) MANE Select	NP_000093.1:p.Asn335Lys