Canonical Allele Identifier: CA471298304
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104595048G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835291G>C , CM000672.2:g.102835291G>C GRCh38
NC_000010.10:g.104595048G>C , CM000672.1:g.104595048G>C GRCh37
NC_000010.9:g.104585038G>C NCBI36
NG_007955.1:g.7243C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.399C>G MANE Select ENSP00000358903.3:p.Ala133=
ENST00000638190.1:c.399C>G ENSP00000492539.1:p.Ala133=
ENST00000638272.1:c.297+1774C>G ENSP00000491508.1:n.297+1774C>G
ENST00000638971.1:c.399C>G ENSP00000492313.1:p.Ala133=
ENST00000639393.1:c.399C>G ENSP00000492651.1:p.Ala133=
ENST00000640633.1:n.161C>G
ENST00000369887.3:c.399C>G ENSP00000358903.3:p.Ala133=
ENST00000489268.1:n.653C>G
NM_000102.3:c.399C>G NP_000093.1:p.Ala133=
NM_000102.4:c.399C>G MANE Select NP_000093.1:p.Ala133=