Canonical Allele Identifier: CA5669591
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1086487
ClinVar RCV Id: RCV001404291
dbSNP Id: rs150698224

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835375C>T , CM000672.2:g.102835375C>T GRCh38
NC_000010.10:g.104595132C>T , CM000672.1:g.104595132C>T GRCh37
NC_000010.9:g.104585122C>T NCBI36
NG_007955.1:g.7159G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.315G>A MANE Select ENSP00000358903.3:p.Ala105=
ENST00000638190.1:c.315G>A ENSP00000492539.1:p.Ala105=
ENST00000638272.1:c.297+1690G>A ENSP00000491508.1:n.297+1690G>A
ENST00000638971.1:c.315G>A ENSP00000492313.1:p.Ala105=
ENST00000639393.1:c.315G>A ENSP00000492651.1:p.Ala105=
ENST00000640633.1:n.77G>A
ENST00000369887.3:c.315G>A ENSP00000358903.3:p.Ala105=
ENST00000489268.1:n.569G>A
NM_000102.3:c.315G>A NP_000093.1:p.Ala105=
NM_000102.4:c.315G>A MANE Select NP_000093.1:p.Ala105=