Canonical Allele Identifier: CA377938253

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1434741428
• gnomAD v2: 10-104590679-C-G
• MyVariant Identifiers: chr10:g.104590679C>G (hg19) ; chr10:g.102830922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830922C>G , CM000672.2:g.102830922C>G	GRCh38
NC_000010.10:g.104590679C>G , CM000672.1:g.104590679C>G	GRCh37
NC_000010.9:g.104580669C>G	NCBI36
NG_007955.1:g.11612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1307G>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly436Ala
ENST00000638190.1:c.1004G>C (CYP17A1)	ENSP00000492539.1:p.Gly335Ala
ENST00000638272.1:c.851G>C (CYP17A1)	ENSP00000491508.1:p.Gly284Ala
ENST00000638971.1:c.1220G>C (CYP17A1)	ENSP00000492313.1:p.Gly407Ala
ENST00000639393.1:c.1310G>C (CYP17A1)	ENSP00000492651.1:p.Gly437Ala
ENST00000640633.1:n.1069G>C (CYP17A1)
ENST00000647664.1:c.*604C>G (WBP1L)	ENSP00000498131.1:n.*604C>G
ENST00000369887.3:c.1307G>C (CYP17A1)	ENSP00000358903.3:p.Gly436Ala
NM_000102.3:c.1307G>C (CYP17A1)	NP_000093.1:p.Gly436Ala
NM_000102.4:c.1307G>C (CYP17A1) MANE Select	NP_000093.1:p.Gly436Ala