Canonical Allele Identifier: CA471287282

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830885-G-C
• MyVariant Identifiers: chr10:g.104590642G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830885G>C , CM000672.2:g.102830885G>C	GRCh38
NC_000010.10:g.104590642G>C , CM000672.1:g.104590642G>C	GRCh37
NC_000010.9:g.104580632G>C	NCBI36
NG_007955.1:g.11649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1344C>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Ala448=
ENST00000638190.1:c.1041C>G (CYP17A1)	ENSP00000492539.1:p.Ala347=
ENST00000638272.1:c.888C>G (CYP17A1)	ENSP00000491508.1:p.Ala296=
ENST00000638971.1:c.1257C>G (CYP17A1)	ENSP00000492313.1:p.Ala419=
ENST00000639393.1:c.1347C>G (CYP17A1)	ENSP00000492651.1:p.Ala449=
ENST00000640633.1:n.1106C>G (CYP17A1)
ENST00000647664.1:c.*567G>C (WBP1L)	ENSP00000498131.1:n.*567G>C
ENST00000369887.3:c.1344C>G (CYP17A1)	ENSP00000358903.3:p.Ala448=
NM_000102.3:c.1344C>G (CYP17A1)	NP_000093.1:p.Ala448=
NM_000102.4:c.1344C>G (CYP17A1) MANE Select	NP_000093.1:p.Ala448=