Canonical Allele Identifier: CA471287339

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590669A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830912A>G , CM000672.2:g.102830912A>G	GRCh38
NC_000010.10:g.104590669A>G , CM000672.1:g.104590669A>G	GRCh37
NC_000010.9:g.104580659A>G	NCBI36
NG_007955.1:g.11622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1317T>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro439=
ENST00000638190.1:c.1014T>C (CYP17A1)	ENSP00000492539.1:p.Pro338=
ENST00000638272.1:c.861T>C (CYP17A1)	ENSP00000491508.1:p.Pro287=
ENST00000638971.1:c.1230T>C (CYP17A1)	ENSP00000492313.1:p.Pro410=
ENST00000639393.1:c.1320T>C (CYP17A1)	ENSP00000492651.1:p.Pro440=
ENST00000640633.1:n.1079T>C (CYP17A1)
ENST00000647664.1:c.*594A>G (WBP1L)	ENSP00000498131.1:n.*594A>G
ENST00000369887.3:c.1317T>C (CYP17A1)	ENSP00000358903.3:p.Pro439=
NM_000102.3:c.1317T>C (CYP17A1)	NP_000093.1:p.Pro439=
NM_000102.4:c.1317T>C (CYP17A1) MANE Select	NP_000093.1:p.Pro439=