Canonical Allele Identifier: CA1932876659

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835107_102835110delinsTAGC , CM000672.2:g.102835107_102835110delinsTAGC	GRCh38
NC_000010.10:g.104594864_104594867delinsTAGC , CM000672.1:g.104594864_104594867delinsTAGC	GRCh37
NC_000010.9:g.104584854_104584857delinsTAGC	NCBI36
NG_007955.1:g.7424_7427delinsGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-96_437-93delinsGCTA MANE Select	ENSP00000358903.3:n.437-96_437-93delinsGCTA
ENST00000638190.1:c.437-96_437-93delinsGCTA	ENSP00000492539.1:n.437-96_437-93delinsGCTA
ENST00000638272.1:c.298-1902_298-1899delinsGCTA	ENSP00000491508.1:n.298-1902_298-1899delinsGCTA
ENST00000638971.1:c.437-96_437-93delinsGCTA	ENSP00000492313.1:n.437-96_437-93delinsGCTA
ENST00000639393.1:c.437-96_437-93delinsGCTA	ENSP00000492651.1:n.437-96_437-93delinsGCTA
ENST00000640633.1:n.199-96_199-93delinsGCTA
ENST00000369887.3:c.437-96_437-93delinsGCTA	ENSP00000358903.3:n.437-96_437-93delinsGCTA
ENST00000489268.1:n.691-96_691-93delinsGCTA
NM_000102.3:c.437-96_437-93delinsGCTA	NP_000093.1:n.437-96_437-93delinsGCTA
NM_000102.4:c.437-96_437-93delinsGCTA MANE Select	NP_000093.1:n.437-96_437-93delinsGCTA