Canonical Allele Identifier: CA377938538

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591323A>T (hg19) ; chr10:g.102831566A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831566A>T , CM000672.2:g.102831566A>T	GRCh38
NC_000010.10:g.104591323A>T , CM000672.1:g.104591323A>T	GRCh37
NC_000010.9:g.104581313A>T	NCBI36
NG_007955.1:g.10968T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1185T>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Asn395Lys
ENST00000638190.1:c.882T>A (CYP17A1)	ENSP00000492539.1:p.Asn294Lys
ENST00000638272.1:c.729T>A (CYP17A1)	ENSP00000491508.1:p.Asn243Lys
ENST00000638971.1:c.1098T>A (CYP17A1)	ENSP00000492313.1:p.Asn366Lys
ENST00000639393.1:c.1188T>A (CYP17A1)	ENSP00000492651.1:p.Asn396Lys
ENST00000640633.1:n.947T>A (CYP17A1)
ENST00000647664.1:c.*629-32A>T (WBP1L)	ENSP00000498131.1:n.*629-32A>T
ENST00000369887.3:c.1185T>A (CYP17A1)	ENSP00000358903.3:p.Asn395Lys
ENST00000469683.1:n.138T>A (CYP17A1)
NM_000102.3:c.1185T>A (CYP17A1)	NP_000093.1:p.Asn395Lys
NM_000102.4:c.1185T>A (CYP17A1) MANE Select	NP_000093.1:p.Asn395Lys