Canonical Allele Identifier: CA471298330

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104595063C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835306C>G , CM000672.2:g.102835306C>G	GRCh38
NC_000010.10:g.104595063C>G , CM000672.1:g.104595063C>G	GRCh37
NC_000010.9:g.104585053C>G	NCBI36
NG_007955.1:g.7228G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.384G>C MANE Select	ENSP00000358903.3:p.Ala128=
ENST00000638190.1:c.384G>C	ENSP00000492539.1:p.Ala128=
ENST00000638272.1:c.297+1759G>C	ENSP00000491508.1:n.297+1759G>C
ENST00000638971.1:c.384G>C	ENSP00000492313.1:p.Ala128=
ENST00000639393.1:c.384G>C	ENSP00000492651.1:p.Ala128=
ENST00000640633.1:n.146G>C
ENST00000369887.3:c.384G>C	ENSP00000358903.3:p.Ala128=
ENST00000489268.1:n.638G>C
NM_000102.3:c.384G>C	NP_000093.1:p.Ala128=
NM_000102.4:c.384G>C MANE Select	NP_000093.1:p.Ala128=