Canonical Allele Identifier: CA2574686221
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835401_102835402del , CM000672.2:g.102835401_102835402del GRCh38
NC_000010.10:g.104595158_104595159del , CM000672.1:g.104595158_104595159del GRCh37
NC_000010.9:g.104585148_104585149del NCBI36
NG_007955.1:g.7136_7137del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.298-6_298-5del MANE Select ENSP00000358903.3:n.298-6_298-5del
ENST00000638190.1:c.298-6_298-5del ENSP00000492539.1:n.298-6_298-5del
ENST00000638272.1:c.297+1667_297+1668del ENSP00000491508.1:n.297+1667_297+1668del
ENST00000638971.1:c.298-6_298-5del ENSP00000492313.1:n.298-6_298-5del
ENST00000639393.1:c.298-6_298-5del ENSP00000492651.1:n.298-6_298-5del
ENST00000640633.1:n.60-6_60-5del
ENST00000369887.3:c.298-6_298-5del ENSP00000358903.3:n.298-6_298-5del
ENST00000489268.1:n.546_547del
NM_000102.3:c.298-6_298-5del NP_000093.1:n.298-6_298-5del
NM_000102.4:c.298-6_298-5del MANE Select NP_000093.1:n.298-6_298-5del