Canonical Allele Identifier: CA2610723822

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833760-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833760T>G , CM000672.2:g.102833760T>G	GRCh38
NC_000010.10:g.104593517T>G , CM000672.1:g.104593517T>G	GRCh37
NC_000010.9:g.104583507T>G	NCBI36
NG_007955.1:g.8774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-417T>G
ENST00000369887.4:c.753+276A>C (CYP17A1) MANE Select	ENSP00000358903.3:n.753+276A>C
ENST00000638190.1:c.666+1025A>C (CYP17A1)	ENSP00000492539.1:n.666+1025A>C
ENST00000638272.1:c.298-552A>C (CYP17A1)	ENSP00000491508.1:n.298-552A>C
ENST00000638971.1:c.667-552A>C (CYP17A1)	ENSP00000492313.1:n.667-552A>C
ENST00000639393.1:c.753+276A>C (CYP17A1)	ENSP00000492651.1:n.753+276A>C
ENST00000640633.1:n.515+276A>C (CYP17A1)
ENST00000647664.1:c.*2791T>G (WBP1L)	ENSP00000498131.1:n.*2791T>G
ENST00000369887.3:c.753+276A>C (CYP17A1)	ENSP00000358903.3:n.753+276A>C
ENST00000489268.1:n.1945A>C (CYP17A1)
NM_000102.3:c.753+276A>C (CYP17A1)	NP_000093.1:n.753+276A>C
XR_428804.1:n.206-417T>G (CYP17A1-AS1)
NM_000102.4:c.753+276A>C (CYP17A1) MANE Select	NP_000093.1:n.753+276A>C