Canonical Allele Identifier: CA377939818

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104594586T>C (hg19) ; chr10:g.102834829T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834829T>C , CM000672.2:g.102834829T>C	GRCh38
NC_000010.10:g.104594586T>C , CM000672.1:g.104594586T>C	GRCh37
NC_000010.9:g.104584576T>C	NCBI36
NG_007955.1:g.7705A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.622A>G MANE Select	ENSP00000358903.3:p.Asn208Asp
ENST00000638190.1:c.622A>G	ENSP00000492539.1:p.Asn208Asp
ENST00000638272.1:c.298-1621A>G	ENSP00000491508.1:n.298-1621A>G
ENST00000638971.1:c.622A>G	ENSP00000492313.1:p.Asn208Asp
ENST00000639393.1:c.622A>G	ENSP00000492651.1:p.Asn208Asp
ENST00000640633.1:n.384A>G
ENST00000369887.3:c.622A>G	ENSP00000358903.3:p.Asn208Asp
ENST00000489268.1:n.876A>G
NM_000102.3:c.622A>G	NP_000093.1:p.Asn208Asp
NM_000102.4:c.622A>G MANE Select	NP_000093.1:p.Asn208Asp