Canonical Allele Identifier: CA377940522
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835382T>G , CM000672.2:g.102835382T>G GRCh38
NC_000010.10:g.104595139T>G , CM000672.1:g.104595139T>G GRCh37
NC_000010.9:g.104585129T>G NCBI36
NG_007955.1:g.7152A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.308A>C MANE Select ENSP00000358903.3:p.Asp103Ala
ENST00000638190.1:c.308A>C ENSP00000492539.1:p.Asp103Ala
ENST00000638272.1:c.297+1683A>C ENSP00000491508.1:n.297+1683A>C
ENST00000638971.1:c.308A>C ENSP00000492313.1:p.Asp103Ala
ENST00000639393.1:c.308A>C ENSP00000492651.1:p.Asp103Ala
ENST00000640633.1:n.70A>C
ENST00000369887.3:c.308A>C ENSP00000358903.3:p.Asp103Ala
ENST00000489268.1:n.562A>C
NM_000102.3:c.308A>C NP_000093.1:p.Asp103Ala
NM_000102.4:c.308A>C MANE Select NP_000093.1:p.Asp103Ala