Canonical Allele Identifier: CA377940082

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104594706A>G (hg19) ; chr10:g.102834949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834949A>G , CM000672.2:g.102834949A>G	GRCh38
NC_000010.10:g.104594706A>G , CM000672.1:g.104594706A>G	GRCh37
NC_000010.9:g.104584696A>G	NCBI36
NG_007955.1:g.7585T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.502T>C MANE Select	ENSP00000358903.3:p.Ser168Pro
ENST00000638190.1:c.502T>C	ENSP00000492539.1:p.Ser168Pro
ENST00000638272.1:c.298-1741T>C	ENSP00000491508.1:n.298-1741T>C
ENST00000638971.1:c.502T>C	ENSP00000492313.1:p.Ser168Pro
ENST00000639393.1:c.502T>C	ENSP00000492651.1:p.Ser168Pro
ENST00000640633.1:n.264T>C
ENST00000369887.3:c.502T>C	ENSP00000358903.3:p.Ser168Pro
ENST00000489268.1:n.756T>C
NM_000102.3:c.502T>C	NP_000093.1:p.Ser168Pro
NM_000102.4:c.502T>C MANE Select	NP_000093.1:p.Ser168Pro