Canonical Allele Identifier: CA377938403

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591267G>C (hg19) ; chr10:g.102831510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831510G>C , CM000672.2:g.102831510G>C	GRCh38
NC_000010.10:g.104591267G>C , CM000672.1:g.104591267G>C	GRCh37
NC_000010.9:g.104581257G>C	NCBI36
NG_007955.1:g.11024C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1241C>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro414Arg
ENST00000638190.1:c.938C>G (CYP17A1)	ENSP00000492539.1:p.Pro313Arg
ENST00000638272.1:c.785C>G (CYP17A1)	ENSP00000491508.1:p.Pro262Arg
ENST00000638971.1:c.1154C>G (CYP17A1)	ENSP00000492313.1:p.Pro385Arg
ENST00000639393.1:c.1244C>G (CYP17A1)	ENSP00000492651.1:p.Pro415Arg
ENST00000640633.1:n.1003C>G (CYP17A1)
ENST00000647664.1:c.*629-88G>C (WBP1L)	ENSP00000498131.1:n.*629-88G>C
ENST00000369887.3:c.1241C>G (CYP17A1)	ENSP00000358903.3:p.Pro414Arg
ENST00000469683.1:n.194C>G (CYP17A1)
NM_000102.3:c.1241C>G (CYP17A1)	NP_000093.1:p.Pro414Arg
NM_000102.4:c.1241C>G (CYP17A1) MANE Select	NP_000093.1:p.Pro414Arg