Canonical Allele Identifier: CA2610724420
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835112del , CM000672.2:g.102835112del GRCh38
NC_000010.10:g.104594869del , CM000672.1:g.104594869del GRCh37
NC_000010.9:g.104584859del NCBI36
NG_007955.1:g.7422del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.437-98del MANE Select ENSP00000358903.3:n.437-98del
ENST00000638190.1:c.437-98del ENSP00000492539.1:n.437-98del
ENST00000638272.1:c.298-1904del ENSP00000491508.1:n.298-1904del
ENST00000638971.1:c.437-98del ENSP00000492313.1:n.437-98del
ENST00000639393.1:c.437-98del ENSP00000492651.1:n.437-98del
ENST00000640633.1:n.199-98del
ENST00000369887.3:c.437-98del ENSP00000358903.3:n.437-98del
ENST00000489268.1:n.691-98del
NM_000102.3:c.437-98del NP_000093.1:n.437-98del
NM_000102.4:c.437-98del MANE Select NP_000093.1:n.437-98del