Canonical Allele Identifier: CA377938416

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591272G>C (hg19) ; chr10:g.102831515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831515G>C , CM000672.2:g.102831515G>C	GRCh38
NC_000010.10:g.104591272G>C , CM000672.1:g.104591272G>C	GRCh37
NC_000010.9:g.104581262G>C	NCBI36
NG_007955.1:g.11019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1236C>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Phe412Leu
ENST00000638190.1:c.933C>G (CYP17A1)	ENSP00000492539.1:p.Phe311Leu
ENST00000638272.1:c.780C>G (CYP17A1)	ENSP00000491508.1:p.Phe260Leu
ENST00000638971.1:c.1149C>G (CYP17A1)	ENSP00000492313.1:p.Phe383Leu
ENST00000639393.1:c.1239C>G (CYP17A1)	ENSP00000492651.1:p.Phe413Leu
ENST00000640633.1:n.998C>G (CYP17A1)
ENST00000647664.1:c.*629-83G>C (WBP1L)	ENSP00000498131.1:n.*629-83G>C
ENST00000369887.3:c.1236C>G (CYP17A1)	ENSP00000358903.3:p.Phe412Leu
ENST00000469683.1:n.189C>G (CYP17A1)
NM_000102.3:c.1236C>G (CYP17A1)	NP_000093.1:p.Phe412Leu
NM_000102.4:c.1236C>G (CYP17A1) MANE Select	NP_000093.1:p.Phe412Leu