Canonical Allele Identifier: CA2610724200

Gene: CYP17A1

Linked Data

• ClinVar Variation Id: 2797536
• ClinVar RCV Id: RCV003673265
• gnomAD v4: 10-102834773-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834773G>A , CM000672.2:g.102834773G>A	GRCh38
NC_000010.10:g.104594530G>A , CM000672.1:g.104594530G>A	GRCh37
NC_000010.9:g.104584520G>A	NCBI36
NG_007955.1:g.7761C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.666+12C>T MANE Select	ENSP00000358903.3:n.666+12C>T
ENST00000638190.1:c.666+12C>T	ENSP00000492539.1:n.666+12C>T
ENST00000638272.1:c.298-1565C>T	ENSP00000491508.1:n.298-1565C>T
ENST00000638971.1:c.666+12C>T	ENSP00000492313.1:n.666+12C>T
ENST00000639393.1:c.666+12C>T	ENSP00000492651.1:n.666+12C>T
ENST00000640633.1:n.428+12C>T
ENST00000369887.3:c.666+12C>T	ENSP00000358903.3:n.666+12C>T
ENST00000489268.1:n.932C>T
NM_000102.3:c.666+12C>T	NP_000093.1:n.666+12C>T
NM_000102.4:c.666+12C>T MANE Select	NP_000093.1:n.666+12C>T