Canonical Allele Identifier: CA471298398

Gene: CYP17A1

Linked Data

• ClinVar Variation Id: 2968697
• ClinVar RCV Id: RCV003829343
• gnomAD v4: 10-102835336-G-T
• MyVariant Identifiers: chr10:g.104595093G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835336G>T , CM000672.2:g.102835336G>T	GRCh38
NC_000010.10:g.104595093G>T , CM000672.1:g.104595093G>T	GRCh37
NC_000010.9:g.104585083G>T	NCBI36
NG_007955.1:g.7198C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.354C>A MANE Select	ENSP00000358903.3:p.Gly118=
ENST00000638190.1:c.354C>A	ENSP00000492539.1:p.Gly118=
ENST00000638272.1:c.297+1729C>A	ENSP00000491508.1:n.297+1729C>A
ENST00000638971.1:c.354C>A	ENSP00000492313.1:p.Gly118=
ENST00000639393.1:c.354C>A	ENSP00000492651.1:p.Gly118=
ENST00000640633.1:n.116C>A
ENST00000369887.3:c.354C>A	ENSP00000358903.3:p.Gly118=
ENST00000489268.1:n.608C>A
NM_000102.3:c.354C>A	NP_000093.1:p.Gly118=
NM_000102.4:c.354C>A MANE Select	NP_000093.1:p.Gly118=