Canonical Allele Identifier: CA2610723964

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102834009-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834012_102834013del , CM000672.2:g.102834012_102834013del	GRCh38
NC_000010.10:g.104593769_104593770del , CM000672.1:g.104593769_104593770del	GRCh37
NC_000010.9:g.104583759_104583760del	NCBI36
NG_007955.1:g.8523_8524del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369884.4:n.152-165_152-164del
ENST00000369887.4:c.753+25_753+26del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+25_753+26del
ENST00000638190.1:c.666+774_666+775del (CYP17A1)	ENSP00000492539.1:n.666+774_666+775del
ENST00000638272.1:c.298-803_298-802del (CYP17A1)	ENSP00000491508.1:n.298-803_298-802del
ENST00000638971.1:c.666+774_666+775del (CYP17A1)	ENSP00000492313.1:n.666+774_666+775del
ENST00000639393.1:c.753+25_753+26del (CYP17A1)	ENSP00000492651.1:n.753+25_753+26del
ENST00000640633.1:n.515+25_515+26del (CYP17A1)
ENST00000369887.3:c.753+25_753+26del (CYP17A1)	ENSP00000358903.3:n.753+25_753+26del
ENST00000489268.1:n.1694_1695del (CYP17A1)
NM_000102.3:c.753+25_753+26del (CYP17A1)	NP_000093.1:n.753+25_753+26del
XR_428804.1:n.206-165_206-164del (CYP17A1-AS1)
NM_000102.4:c.753+25_753+26del (CYP17A1) MANE Select	NP_000093.1:n.753+25_753+26del