Canonical Allele Identifier: CA659060419

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1158953435
• gnomAD v3: 10-102836615-AG-A
• gnomAD v4: 10-102836615-AG-A
• MyVariant Identifiers: chr10:g.104596373del (hg19) ; chr10:g.102836616del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836617del , CM000672.2:g.102836617del	GRCh38
NC_000010.10:g.104596374del , CM000672.1:g.104596374del	GRCh37
NC_000010.9:g.104586364del	NCBI36
NG_007955.1:g.5918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+449del MANE Select	ENSP00000358903.3:n.297+449del
ENST00000638190.1:c.297+449del	ENSP00000492539.1:n.297+449del
ENST00000638272.1:c.297+449del	ENSP00000491508.1:n.297+449del
ENST00000638971.1:c.297+449del	ENSP00000492313.1:n.297+449del
ENST00000639393.1:c.297+449del	ENSP00000492651.1:n.297+449del
ENST00000640633.1:n.59+98del
ENST00000369887.3:c.297+449del	ENSP00000358903.3:n.297+449del
ENST00000489268.1:n.350+449del
NM_000102.3:c.297+449del	NP_000093.1:n.297+449del
NM_000102.4:c.297+449del MANE Select	NP_000093.1:n.297+449del