Canonical Allele Identifier: CA377939869

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104594609T>C (hg19) ; chr10:g.102834852T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834852T>C , CM000672.2:g.102834852T>C	GRCh38
NC_000010.10:g.104594609T>C , CM000672.1:g.104594609T>C	GRCh37
NC_000010.9:g.104584599T>C	NCBI36
NG_007955.1:g.7682A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.599A>G MANE Select	ENSP00000358903.3:p.Asn200Ser
ENST00000638190.1:c.599A>G	ENSP00000492539.1:p.Asn200Ser
ENST00000638272.1:c.298-1644A>G	ENSP00000491508.1:n.298-1644A>G
ENST00000638971.1:c.599A>G	ENSP00000492313.1:p.Asn200Ser
ENST00000639393.1:c.599A>G	ENSP00000492651.1:p.Asn200Ser
ENST00000640633.1:n.361A>G
ENST00000369887.3:c.599A>G	ENSP00000358903.3:p.Asn200Ser
ENST00000489268.1:n.853A>G
NM_000102.3:c.599A>G	NP_000093.1:p.Asn200Ser
NM_000102.4:c.599A>G MANE Select	NP_000093.1:p.Asn200Ser