Canonical Allele Identifier: CA377940001
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104594666A>T (hg19) chr10:g.102834909A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834909A>T , CM000672.2:g.102834909A>T GRCh38
NC_000010.10:g.104594666A>T , CM000672.1:g.104594666A>T GRCh37
NC_000010.9:g.104584656A>T NCBI36
NG_007955.1:g.7625T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.542T>A MANE Select ENSP00000358903.3:p.Leu181Ter
ENST00000638190.1:c.542T>A ENSP00000492539.1:p.Leu181Ter
ENST00000638272.1:c.298-1701T>A ENSP00000491508.1:n.298-1701T>A
ENST00000638971.1:c.542T>A ENSP00000492313.1:p.Leu181Ter
ENST00000639393.1:c.542T>A ENSP00000492651.1:p.Leu181Ter
ENST00000640633.1:n.304T>A
ENST00000369887.3:c.542T>A ENSP00000358903.3:p.Leu181Ter
ENST00000489268.1:n.796T>A
NM_000102.3:c.542T>A NP_000093.1:p.Leu181Ter
NM_000102.4:c.542T>A MANE Select NP_000093.1:p.Leu181Ter
Search 100 bp 5'
Search 100 bp 3'