Canonical Allele Identifier: CA377938371

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590734A>T (hg19) ; chr10:g.102830977A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830977A>T , CM000672.2:g.102830977A>T	GRCh38
NC_000010.10:g.104590734A>T , CM000672.1:g.104590734A>T	GRCh37
NC_000010.9:g.104580724A>T	NCBI36
NG_007955.1:g.11557T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1252T>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu418Met
ENST00000638190.1:c.949T>A (CYP17A1)	ENSP00000492539.1:p.Leu317Met
ENST00000638272.1:c.796T>A (CYP17A1)	ENSP00000491508.1:p.Leu266Met
ENST00000638971.1:c.1165T>A (CYP17A1)	ENSP00000492313.1:p.Leu389Met
ENST00000639393.1:c.1255T>A (CYP17A1)	ENSP00000492651.1:p.Leu419Met
ENST00000640633.1:n.1014T>A (CYP17A1)
ENST00000647664.1:c.*628+31A>T (WBP1L)	ENSP00000498131.1:n.*628+31A>T
ENST00000369887.3:c.1252T>A (CYP17A1)	ENSP00000358903.3:p.Leu418Met
ENST00000469683.1:n.205T>A (CYP17A1)
NM_000102.3:c.1252T>A (CYP17A1)	NP_000093.1:p.Leu418Met
NM_000102.4:c.1252T>A (CYP17A1) MANE Select	NP_000093.1:p.Leu418Met