Canonical Allele Identifier: CA471298312
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104595051A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835294A>G , CM000672.2:g.102835294A>G GRCh38
NC_000010.10:g.104595051A>G , CM000672.1:g.104595051A>G GRCh37
NC_000010.9:g.104585041A>G NCBI36
NG_007955.1:g.7240T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.396T>C MANE Select ENSP00000358903.3:p.Phe132=
ENST00000638190.1:c.396T>C ENSP00000492539.1:p.Phe132=
ENST00000638272.1:c.297+1771T>C ENSP00000491508.1:n.297+1771T>C
ENST00000638971.1:c.396T>C ENSP00000492313.1:p.Phe132=
ENST00000639393.1:c.396T>C ENSP00000492651.1:p.Phe132=
ENST00000640633.1:n.158T>C
ENST00000369887.3:c.396T>C ENSP00000358903.3:p.Phe132=
ENST00000489268.1:n.650T>C
NM_000102.3:c.396T>C NP_000093.1:p.Phe132=
NM_000102.4:c.396T>C MANE Select NP_000093.1:p.Phe132=