Canonical Allele Identifier: CA1932839930

Gene: CYP17A1

Linked Data

• dbSNP Id: rs3781287

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835663T>A , CM000672.2:g.102835663T>A	GRCh38
NC_000010.10:g.104595420T>A , CM000672.1:g.104595420T>A	GRCh37
NC_000010.9:g.104585410T>A	NCBI36
NG_007955.1:g.6871A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.298-271A>T MANE Select	ENSP00000358903.3:n.298-271A>T
ENST00000638190.1:c.298-271A>T	ENSP00000492539.1:n.298-271A>T
ENST00000638272.1:c.297+1402A>T	ENSP00000491508.1:n.297+1402A>T
ENST00000638971.1:c.298-271A>T	ENSP00000492313.1:n.298-271A>T
ENST00000639393.1:c.298-271A>T	ENSP00000492651.1:n.298-271A>T
ENST00000640633.1:n.60-271A>T
ENST00000369887.3:c.298-271A>T	ENSP00000358903.3:n.298-271A>T
ENST00000489268.1:n.351-70A>T
NM_000102.3:c.298-271A>T	NP_000093.1:n.298-271A>T
NM_000102.4:c.298-271A>T MANE Select	NP_000093.1:n.298-271A>T