Canonical Allele Identifier: CA2610723865

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833835-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833835G>A , CM000672.2:g.102833835G>A	GRCh38
NC_000010.10:g.104593592G>A , CM000672.1:g.104593592G>A	GRCh37
NC_000010.9:g.104583582G>A	NCBI36
NG_007955.1:g.8699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-342G>A
ENST00000369887.4:c.753+201C>T (CYP17A1) MANE Select	ENSP00000358903.3:n.753+201C>T
ENST00000638190.1:c.666+950C>T (CYP17A1)	ENSP00000492539.1:n.666+950C>T
ENST00000638272.1:c.298-627C>T (CYP17A1)	ENSP00000491508.1:n.298-627C>T
ENST00000638971.1:c.667-627C>T (CYP17A1)	ENSP00000492313.1:n.667-627C>T
ENST00000639393.1:c.753+201C>T (CYP17A1)	ENSP00000492651.1:n.753+201C>T
ENST00000640633.1:n.515+201C>T (CYP17A1)
ENST00000647664.1:c.*2866G>A (WBP1L)	ENSP00000498131.1:n.*2866G>A
ENST00000369887.3:c.753+201C>T (CYP17A1)	ENSP00000358903.3:n.753+201C>T
ENST00000489268.1:n.1870C>T (CYP17A1)
NM_000102.3:c.753+201C>T (CYP17A1)	NP_000093.1:n.753+201C>T
XR_428804.1:n.206-342G>A (CYP17A1-AS1)
NM_000102.4:c.753+201C>T (CYP17A1) MANE Select	NP_000093.1:n.753+201C>T