Canonical Allele Identifier: CA471297460

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104594590T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834833T>G , CM000672.2:g.102834833T>G	GRCh38
NC_000010.10:g.104594590T>G , CM000672.1:g.104594590T>G	GRCh37
NC_000010.9:g.104584580T>G	NCBI36
NG_007955.1:g.7701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.618A>C MANE Select	ENSP00000358903.3:p.Ile206=
ENST00000638190.1:c.618A>C	ENSP00000492539.1:p.Ile206=
ENST00000638272.1:c.298-1625A>C	ENSP00000491508.1:n.298-1625A>C
ENST00000638971.1:c.618A>C	ENSP00000492313.1:p.Ile206=
ENST00000639393.1:c.618A>C	ENSP00000492651.1:p.Ile206=
ENST00000640633.1:n.380A>C
ENST00000369887.3:c.618A>C	ENSP00000358903.3:p.Ile206=
ENST00000489268.1:n.872A>C
NM_000102.3:c.618A>C	NP_000093.1:p.Ile206=
NM_000102.4:c.618A>C MANE Select	NP_000093.1:p.Ile206=