Canonical Allele Identifier: CA377940031

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844140050
• gnomAD v3: 10-102834924-G-T
• gnomAD v4: 10-102834924-G-T
• MyVariant Identifiers: chr10:g.104594681G>T (hg19) ; chr10:g.102834924G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834924G>T , CM000672.2:g.102834924G>T	GRCh38
NC_000010.10:g.104594681G>T , CM000672.1:g.104594681G>T	GRCh37
NC_000010.9:g.104584671G>T	NCBI36
NG_007955.1:g.7610C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.527C>A MANE Select	ENSP00000358903.3:p.Thr176Asn
ENST00000638190.1:c.527C>A	ENSP00000492539.1:p.Thr176Asn
ENST00000638272.1:c.298-1716C>A	ENSP00000491508.1:n.298-1716C>A
ENST00000638971.1:c.527C>A	ENSP00000492313.1:p.Thr176Asn
ENST00000639393.1:c.527C>A	ENSP00000492651.1:p.Thr176Asn
ENST00000640633.1:n.289C>A
ENST00000369887.3:c.527C>A	ENSP00000358903.3:p.Thr176Asn
ENST00000489268.1:n.781C>A
NM_000102.3:c.527C>A	NP_000093.1:p.Thr176Asn
NM_000102.4:c.527C>A MANE Select	NP_000093.1:p.Thr176Asn