Canonical Allele Identifier: CA471297478

Gene: CYP17A1

Linked Data

• ClinVar Variation Id: 2030587
• ClinVar RCV Id: RCV002871854
• MyVariant Identifiers: chr10:g.104594596G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834839G>C , CM000672.2:g.102834839G>C	GRCh38
NC_000010.10:g.104594596G>C , CM000672.1:g.104594596G>C	GRCh37
NC_000010.9:g.104584586G>C	NCBI36
NG_007955.1:g.7695C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.612C>G MANE Select	ENSP00000358903.3:p.Gly204=
ENST00000638190.1:c.612C>G	ENSP00000492539.1:p.Gly204=
ENST00000638272.1:c.298-1631C>G	ENSP00000491508.1:n.298-1631C>G
ENST00000638971.1:c.612C>G	ENSP00000492313.1:p.Gly204=
ENST00000639393.1:c.612C>G	ENSP00000492651.1:p.Gly204=
ENST00000640633.1:n.374C>G
ENST00000369887.3:c.612C>G	ENSP00000358903.3:p.Gly204=
ENST00000489268.1:n.866C>G
NM_000102.3:c.612C>G	NP_000093.1:p.Gly204=
NM_000102.4:c.612C>G MANE Select	NP_000093.1:p.Gly204=