Canonical Allele Identifier: CA3003424026

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835221A>C , CM000672.2:g.102835221A>C	GRCh38
NC_000010.10:g.104594978A>C , CM000672.1:g.104594978A>C	GRCh37
NC_000010.9:g.104584968A>C	NCBI36
NG_007955.1:g.7313T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+33T>G MANE Select	ENSP00000358903.3:n.436+33T>G
ENST00000638190.1:c.436+33T>G	ENSP00000492539.1:n.436+33T>G
ENST00000638272.1:c.297+1844T>G	ENSP00000491508.1:n.297+1844T>G
ENST00000638971.1:c.436+33T>G	ENSP00000492313.1:n.436+33T>G
ENST00000639393.1:c.436+33T>G	ENSP00000492651.1:n.436+33T>G
ENST00000640633.1:n.198+33T>G
ENST00000369887.3:c.436+33T>G	ENSP00000358903.3:n.436+33T>G
ENST00000489268.1:n.690+33T>G
NM_000102.3:c.436+33T>G	NP_000093.1:n.436+33T>G
NM_000102.4:c.436+33T>G MANE Select	NP_000093.1:n.436+33T>G