Canonical Allele Identifier: CA1932875783

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834814_102834815delinsTG , CM000672.2:g.102834814_102834815delinsTG	GRCh38
NC_000010.10:g.104594571_104594572delinsTG , CM000672.1:g.104594571_104594572delinsTG	GRCh37
NC_000010.9:g.104584561_104584562delinsTG	NCBI36
NG_007955.1:g.7719_7720delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.636_637delinsCA MANE Select	ENSP00000358903.3:p.Asp212=
ENST00000638190.1:c.636_637delinsCA	ENSP00000492539.1:p.Asp212=
ENST00000638272.1:c.298-1607_298-1606delinsCA	ENSP00000491508.1:n.298-1607_298-1606delinsCA
ENST00000638971.1:c.636_637delinsCA	ENSP00000492313.1:p.Asp212=
ENST00000639393.1:c.636_637delinsCA	ENSP00000492651.1:p.Asp212=
ENST00000640633.1:n.398_399delinsCA
ENST00000369887.3:c.636_637delinsCA	ENSP00000358903.3:p.Asp212=
ENST00000489268.1:n.890_891delinsCA
NM_000102.3:c.636_637delinsCA	NP_000093.1:p.Asp212=
NM_000102.4:c.636_637delinsCA MANE Select	NP_000093.1:p.Asp212=