Canonical Allele Identifier: CA377939526
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 10-102834040-T-A
MyVariant Identifiers: chr10:g.104593797T>A (hg19) chr10:g.102834040T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834040T>A , CM000672.2:g.102834040T>A GRCh38
NC_000010.10:g.104593797T>A , CM000672.1:g.104593797T>A GRCh37
NC_000010.9:g.104583787T>A NCBI36
NG_007955.1:g.8494A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-137T>A
ENST00000369887.4:c.749A>T (CYP17A1) MANE Select ENSP00000358903.3:p.Tyr250Phe
ENST00000638190.1:c.666+745A>T (CYP17A1) ENSP00000492539.1:n.666+745A>T
ENST00000638272.1:c.298-832A>T (CYP17A1) ENSP00000491508.1:n.298-832A>T
ENST00000638971.1:c.666+745A>T (CYP17A1) ENSP00000492313.1:n.666+745A>T
ENST00000639393.1:c.749A>T (CYP17A1) ENSP00000492651.1:p.Tyr250Phe
ENST00000640633.1:n.511A>T (CYP17A1)
ENST00000369887.3:c.749A>T (CYP17A1) ENSP00000358903.3:p.Tyr250Phe
ENST00000489268.1:n.1665A>T (CYP17A1)
NM_000102.3:c.749A>T (CYP17A1) NP_000093.1:p.Tyr250Phe
XR_428804.1:n.206-137T>A (CYP17A1-AS1)
NM_000102.4:c.749A>T (CYP17A1) MANE Select NP_000093.1:p.Tyr250Phe
Search 100 bp 5'
Search 100 bp 3'