Canonical Allele Identifier: CA377939563
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1844126437

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834055T>G , CM000672.2:g.102834055T>G GRCh38
NC_000010.10:g.104593812T>G , CM000672.1:g.104593812T>G GRCh37
NC_000010.9:g.104583802T>G NCBI36
NG_007955.1:g.8479A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-122T>G
ENST00000369887.4:c.734A>C (CYP17A1) MANE Select ENSP00000358903.3:p.Lys245Thr
ENST00000638190.1:c.666+730A>C (CYP17A1) ENSP00000492539.1:n.666+730A>C
ENST00000638272.1:c.298-847A>C (CYP17A1) ENSP00000491508.1:n.298-847A>C
ENST00000638971.1:c.666+730A>C (CYP17A1) ENSP00000492313.1:n.666+730A>C
ENST00000639393.1:c.734A>C (CYP17A1) ENSP00000492651.1:p.Lys245Thr
ENST00000640633.1:n.496A>C (CYP17A1)
ENST00000369887.3:c.734A>C (CYP17A1) ENSP00000358903.3:p.Lys245Thr
ENST00000489268.1:n.1650A>C (CYP17A1)
NM_000102.3:c.734A>C (CYP17A1) NP_000093.1:p.Lys245Thr
XR_428804.1:n.206-122T>G (CYP17A1-AS1)
NM_000102.4:c.734A>C (CYP17A1) MANE Select NP_000093.1:p.Lys245Thr