Canonical Allele Identifier: CA1932839737
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835406_102835407delinsGC , CM000672.2:g.102835406_102835407delinsGC GRCh38
NC_000010.10:g.104595163_104595164delinsGC , CM000672.1:g.104595163_104595164delinsGC GRCh37
NC_000010.9:g.104585153_104585154delinsGC NCBI36
NG_007955.1:g.7127_7128delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.298-15_298-14delinsGC MANE Select ENSP00000358903.3:n.298-15_298-14delinsGC...
ENST00000638190.1:c.298-15_298-14delinsGC ENSP00000492539.1:n.298-15_298-14delinsGC...
ENST00000638272.1:c.297+1658_297+1659delinsGC ENSP00000491508.1:n.297+1658_297+1659deli...
ENST00000638971.1:c.298-15_298-14delinsGC ENSP00000492313.1:n.298-15_298-14delinsGC...
ENST00000639393.1:c.298-15_298-14delinsGC ENSP00000492651.1:n.298-15_298-14delinsGC...
ENST00000640633.1:n.60-15_60-14delinsGC
ENST00000369887.3:c.298-15_298-14delinsGC ENSP00000358903.3:n.298-15_298-14delinsGC...
ENST00000489268.1:n.537_538delinsGC
NM_000102.3:c.298-15_298-14delinsGC NP_000093.1:n.298-15_298-14delinsGC
NM_000102.4:c.298-15_298-14delinsGC MANE Select NP_000093.1:n.298-15_298-14delinsGC