Canonical Allele Identifier: CA377938552

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591329G>C (hg19) ; chr10:g.102831572G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831572G>C , CM000672.2:g.102831572G>C	GRCh38
NC_000010.10:g.104591329G>C , CM000672.1:g.104591329G>C	GRCh37
NC_000010.9:g.104581319G>C	NCBI36
NG_007955.1:g.10962C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1179C>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Ile393Met
ENST00000638190.1:c.876C>G (CYP17A1)	ENSP00000492539.1:p.Ile292Met
ENST00000638272.1:c.723C>G (CYP17A1)	ENSP00000491508.1:p.Ile241Met
ENST00000638971.1:c.1092C>G (CYP17A1)	ENSP00000492313.1:p.Ile364Met
ENST00000639393.1:c.1182C>G (CYP17A1)	ENSP00000492651.1:p.Ile394Met
ENST00000640633.1:n.941C>G (CYP17A1)
ENST00000647664.1:c.*629-26G>C (WBP1L)	ENSP00000498131.1:n.*629-26G>C
ENST00000369887.3:c.1179C>G (CYP17A1)	ENSP00000358903.3:p.Ile393Met
ENST00000469683.1:n.132C>G (CYP17A1)
NM_000102.3:c.1179C>G (CYP17A1)	NP_000093.1:p.Ile393Met
NM_000102.4:c.1179C>G (CYP17A1) MANE Select	NP_000093.1:p.Ile393Met