Canonical Allele Identifier: CA212294279

Gene: CYP17A1

Linked Data

• dbSNP Id: rs780472449
• gnomAD v4: 10-102835125-T-C
• COSMIC: COSN8638977
• MyVariant Identifiers: chr10:g.104594882T>C (hg19) ; chr10:g.102835125T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835125T>C , CM000672.2:g.102835125T>C	GRCh38
NC_000010.10:g.104594882T>C , CM000672.1:g.104594882T>C	GRCh37
NC_000010.9:g.104584872T>C	NCBI36
NG_007955.1:g.7409A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-111A>G MANE Select	ENSP00000358903.3:n.437-111A>G
ENST00000638190.1:c.437-111A>G	ENSP00000492539.1:n.437-111A>G
ENST00000638272.1:c.298-1917A>G	ENSP00000491508.1:n.298-1917A>G
ENST00000638971.1:c.437-111A>G	ENSP00000492313.1:n.437-111A>G
ENST00000639393.1:c.437-111A>G	ENSP00000492651.1:n.437-111A>G
ENST00000640633.1:n.199-111A>G
ENST00000369887.3:c.437-111A>G	ENSP00000358903.3:n.437-111A>G
ENST00000489268.1:n.691-111A>G
NM_000102.3:c.437-111A>G	NP_000093.1:n.437-111A>G
NM_000102.4:c.437-111A>G MANE Select	NP_000093.1:n.437-111A>G