Canonical Allele Identifier: CA1932876632
Gene: CYP17A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835098G= , CM000672.2:g.102835098G= GRCh38
NC_000010.10:g.104594855G= , CM000672.1:g.104594855G= GRCh37
NC_000010.9:g.104584845G= NCBI36
NG_007955.1:g.7436C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.437-84C= MANE Select ENSP00000358903.3:n.437-84C=
ENST00000638190.1:c.437-84C= ENSP00000492539.1:n.437-84C=
ENST00000638272.1:c.298-1890C= ENSP00000491508.1:n.298-1890C=
ENST00000638971.1:c.437-84C= ENSP00000492313.1:n.437-84C=
ENST00000639393.1:c.437-84C= ENSP00000492651.1:n.437-84C=
ENST00000640633.1:n.199-84C=
ENST00000369887.3:c.437-84C= ENSP00000358903.3:n.437-84C=
ENST00000489268.1:n.691-84C=
NM_000102.3:c.437-84C= NP_000093.1:n.437-84C=
NM_000102.4:c.437-84C= MANE Select NP_000093.1:n.437-84C=
Search 100 bp 5'
Search 100 bp 3'