Canonical Allele Identifier: CA1932839739

Gene: CYP17A1

Linked Data

• ClinVar Variation Id: 2830355
• ClinVar RCV Id: RCV003694174
• dbSNP Id: rs1844150752
• gnomAD v4: 10-102835407-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835407C>A , CM000672.2:g.102835407C>A	GRCh38
NC_000010.10:g.104595164C>A , CM000672.1:g.104595164C>A	GRCh37
NC_000010.9:g.104585154C>A	NCBI36
NG_007955.1:g.7127G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.298-15G>T MANE Select	ENSP00000358903.3:n.298-15G>T
ENST00000638190.1:c.298-15G>T	ENSP00000492539.1:n.298-15G>T
ENST00000638272.1:c.297+1658G>T	ENSP00000491508.1:n.297+1658G>T
ENST00000638971.1:c.298-15G>T	ENSP00000492313.1:n.298-15G>T
ENST00000639393.1:c.298-15G>T	ENSP00000492651.1:n.298-15G>T
ENST00000640633.1:n.60-15G>T
ENST00000369887.3:c.298-15G>T	ENSP00000358903.3:n.298-15G>T
ENST00000489268.1:n.537G>T
NM_000102.3:c.298-15G>T	NP_000093.1:n.298-15G>T
NM_000102.4:c.298-15G>T MANE Select	NP_000093.1:n.298-15G>T