Canonical Allele Identifier: CA1932839453
Gene: CYP17A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835182C= , CM000672.2:g.102835182C= GRCh38
NC_000010.10:g.104594939C= , CM000672.1:g.104594939C= GRCh37
NC_000010.9:g.104584929C= NCBI36
NG_007955.1:g.7352G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.436+72G= MANE Select ENSP00000358903.3:n.436+72G=
ENST00000638190.1:c.436+72G= ENSP00000492539.1:n.436+72G=
ENST00000638272.1:c.297+1883G= ENSP00000491508.1:n.297+1883G=
ENST00000638971.1:c.436+72G= ENSP00000492313.1:n.436+72G=
ENST00000639393.1:c.436+72G= ENSP00000492651.1:n.436+72G=
ENST00000640633.1:n.198+72G=
ENST00000369887.3:c.436+72G= ENSP00000358903.3:n.436+72G=
ENST00000489268.1:n.690+72G=
NM_000102.3:c.436+72G= NP_000093.1:n.436+72G=
NM_000102.4:c.436+72G= MANE Select NP_000093.1:n.436+72G=
Search 100 bp 5'
Search 100 bp 3'