Canonical Allele Identifier: CA212294280

Gene: CYP17A1

Linked Data

• dbSNP Id: rs980336663
• gnomAD v4: 10-102835127-G-A
• MyVariant Identifiers: chr10:g.104594884G>A (hg19) ; chr10:g.102835127G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835127G>A , CM000672.2:g.102835127G>A	GRCh38
NC_000010.10:g.104594884G>A , CM000672.1:g.104594884G>A	GRCh37
NC_000010.9:g.104584874G>A	NCBI36
NG_007955.1:g.7407C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-113C>T MANE Select	ENSP00000358903.3:n.437-113C>T
ENST00000638190.1:c.437-113C>T	ENSP00000492539.1:n.437-113C>T
ENST00000638272.1:c.298-1919C>T	ENSP00000491508.1:n.298-1919C>T
ENST00000638971.1:c.437-113C>T	ENSP00000492313.1:n.437-113C>T
ENST00000639393.1:c.437-113C>T	ENSP00000492651.1:n.437-113C>T
ENST00000640633.1:n.199-113C>T
ENST00000369887.3:c.437-113C>T	ENSP00000358903.3:n.437-113C>T
ENST00000489268.1:n.691-113C>T
NM_000102.3:c.437-113C>T	NP_000093.1:n.437-113C>T
NM_000102.4:c.437-113C>T MANE Select	NP_000093.1:n.437-113C>T