Canonical Allele Identifier: CA2610725952
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837515_102837516insGCCTGGCTGGGCT , CM000672.2:g.102837515_102837516insGCCTGGCTGGGCT GRCh38
NC_000010.10:g.104597272_104597273insGCCTGGCTGGGCT , CM000672.1:g.104597272_104597273insGCCTGGCTGGGCT GRCh37
NC_000010.9:g.104587262_104587263insGCCTGGCTGGGCT NCBI36
NG_007955.1:g.5018_5019insAGCCCAGCCAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.3:c.-155_-154insAGCCCAGCCAGGC ENSP00000358903.3:n.-155_-154insAGCCCAGCCAGGC
NM_000102.3:c.-155_-154insAGCCCAGCCAGGC NP_000093.1:n.-155_-154insAGCCCAGCCAGGC