Canonical Allele Identifier: CA5669660

Gene: CYP17A1

Linked Data

• dbSNP Id: rs773741105
• ExAC: 10:104597074 CA / C
• gnomAD v2: 10-104597074-CA-C
• gnomAD v4: 10-102837317-CA-C
• MyVariant Identifiers: chr10:g.104597075del (hg19) ; chr10:g.102837318del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837320del , CM000672.2:g.102837320del	GRCh38
NC_000010.10:g.104597077del , CM000672.1:g.104597077del	GRCh37
NC_000010.9:g.104587067del	NCBI36
NG_007955.1:g.5216del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.44del MANE Select	ENSP00000358903.3:p.Leu15CysfsTer?
ENST00000638190.1:c.44del	ENSP00000492539.1:p.Leu15CysfsTer?
ENST00000638272.1:c.44del	ENSP00000491508.1:p.Leu15CysfsTer?
ENST00000638971.1:c.44del	ENSP00000492313.1:p.Leu15CysfsTer?
ENST00000639393.1:c.44del	ENSP00000492651.1:p.Leu15CysfsTer?
ENST00000369887.3:c.44del	ENSP00000358903.3:p.Leu15CysfsTer?
ENST00000489268.1:n.97del
NM_000102.3:c.44del	NP_000093.1:p.Leu15CysfsTer?
NM_000102.4:c.44del MANE Select	NP_000093.1:p.Leu15CysfsTer?