Canonical Allele Identifier: CA471287486

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830975-C-T
• MyVariant Identifiers: chr10:g.104590732C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830975C>T , CM000672.2:g.102830975C>T	GRCh38
NC_000010.10:g.104590732C>T , CM000672.1:g.104590732C>T	GRCh37
NC_000010.9:g.104580722C>T	NCBI36
NG_007955.1:g.11559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1254G>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu418=
ENST00000638190.1:c.951G>A (CYP17A1)	ENSP00000492539.1:p.Leu317=
ENST00000638272.1:c.798G>A (CYP17A1)	ENSP00000491508.1:p.Leu266=
ENST00000638971.1:c.1167G>A (CYP17A1)	ENSP00000492313.1:p.Leu389=
ENST00000639393.1:c.1257G>A (CYP17A1)	ENSP00000492651.1:p.Leu419=
ENST00000640633.1:n.1016G>A (CYP17A1)
ENST00000647664.1:c.*628+29C>T (WBP1L)	ENSP00000498131.1:n.*628+29C>T
ENST00000369887.3:c.1254G>A (CYP17A1)	ENSP00000358903.3:p.Leu418=
ENST00000469683.1:n.207G>A (CYP17A1)
NM_000102.3:c.1254G>A (CYP17A1)	NP_000093.1:p.Leu418=
NM_000102.4:c.1254G>A (CYP17A1) MANE Select	NP_000093.1:p.Leu418=