Canonical Allele Identifier: CA1932839529
Gene: CYP17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835238C= , CM000672.2:g.102835238C= GRCh38
NC_000010.10:g.104594995C= , CM000672.1:g.104594995C= GRCh37
NC_000010.9:g.104584985C= NCBI36
NG_007955.1:g.7296G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.436+16G= MANE Select ENSP00000358903.3:n.436+16G=
ENST00000638190.1:c.436+16G= ENSP00000492539.1:n.436+16G=
ENST00000638272.1:c.297+1827G= ENSP00000491508.1:n.297+1827G=
ENST00000638971.1:c.436+16G= ENSP00000492313.1:n.436+16G=
ENST00000639393.1:c.436+16G= ENSP00000492651.1:n.436+16G=
ENST00000640633.1:n.198+16G=
ENST00000369887.3:c.436+16G= ENSP00000358903.3:n.436+16G=
ENST00000489268.1:n.690+16G=
NM_000102.3:c.436+16G= NP_000093.1:n.436+16G=
NM_000102.4:c.436+16G= MANE Select NP_000093.1:n.436+16G=
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