Canonical Allele Identifier: CA1932839544
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835256_102835259delinsATCT , CM000672.2:g.102835256_102835259delinsATCT GRCh38
NC_000010.10:g.104595013_104595016delinsATCT , CM000672.1:g.104595013_104595016delinsATCT GRCh37
NC_000010.9:g.104585003_104585006delinsATCT NCBI36
NG_007955.1:g.7275_7278delinsAGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.431_434delinsAGAT MANE Select ENSP00000358903.3:p.Lys144=
ENST00000638190.1:c.431_434delinsAGAT ENSP00000492539.1:p.Lys144=
ENST00000638272.1:c.297+1806_297+1809delinsAGAT ENSP00000491508.1:n.297+1806_297+1809deli...
ENST00000638971.1:c.431_434delinsAGAT ENSP00000492313.1:p.Lys144=
ENST00000639393.1:c.431_434delinsAGAT ENSP00000492651.1:p.Lys144=
ENST00000640633.1:n.193_196delinsAGAT
ENST00000369887.3:c.431_434delinsAGAT ENSP00000358903.3:p.Lys144=
ENST00000489268.1:n.685_688delinsAGAT
NM_000102.3:c.431_434delinsAGAT NP_000093.1:p.Lys144=
NM_000102.4:c.431_434delinsAGAT MANE Select NP_000093.1:p.Lys144=