Canonical Allele Identifier: CA595226480

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1317479062
• gnomAD v2: 10-104596535-CAG-C
• gnomAD v3: 10-102836778-CAG-C
• gnomAD v4: 10-102836778-CAG-C
• MyVariant Identifiers: chr10:g.104596536_104596537del (hg19) ; chr10:g.102836779_102836780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836785_102836786del , CM000672.2:g.102836785_102836786del	GRCh38
NC_000010.10:g.104596542_104596543del , CM000672.1:g.104596542_104596543del	GRCh37
NC_000010.9:g.104586532_104586533del	NCBI36
NG_007955.1:g.5754_5755del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+285_297+286del MANE Select	ENSP00000358903.3:n.297+285_297+286del
ENST00000638190.1:c.297+285_297+286del	ENSP00000492539.1:n.297+285_297+286del
ENST00000638272.1:c.297+285_297+286del	ENSP00000491508.1:n.297+285_297+286del
ENST00000638971.1:c.297+285_297+286del	ENSP00000492313.1:n.297+285_297+286del
ENST00000639393.1:c.297+285_297+286del	ENSP00000492651.1:n.297+285_297+286del
ENST00000369887.3:c.297+285_297+286del	ENSP00000358903.3:n.297+285_297+286del
ENST00000489268.1:n.350+285_350+286del
NM_000102.3:c.297+285_297+286del	NP_000093.1:n.297+285_297+286del
NM_000102.4:c.297+285_297+286del MANE Select	NP_000093.1:n.297+285_297+286del