Canonical Allele Identifier: CA377938378

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590737A>G (hg19) ; chr10:g.102830980A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830980A>G , CM000672.2:g.102830980A>G	GRCh38
NC_000010.10:g.104590737A>G , CM000672.1:g.104590737A>G	GRCh37
NC_000010.9:g.104580727A>G	NCBI36
NG_007955.1:g.11554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1249T>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Phe417Leu
ENST00000638190.1:c.946T>C (CYP17A1)	ENSP00000492539.1:p.Phe316Leu
ENST00000638272.1:c.793T>C (CYP17A1)	ENSP00000491508.1:p.Phe265Leu
ENST00000638971.1:c.1162T>C (CYP17A1)	ENSP00000492313.1:p.Phe388Leu
ENST00000639393.1:c.1252T>C (CYP17A1)	ENSP00000492651.1:p.Phe418Leu
ENST00000640633.1:n.1011T>C (CYP17A1)
ENST00000647664.1:c.*628+34A>G (WBP1L)	ENSP00000498131.1:n.*628+34A>G
ENST00000369887.3:c.1249T>C (CYP17A1)	ENSP00000358903.3:p.Phe417Leu
ENST00000469683.1:n.202T>C (CYP17A1)
NM_000102.3:c.1249T>C (CYP17A1)	NP_000093.1:p.Phe417Leu
NM_000102.4:c.1249T>C (CYP17A1) MANE Select	NP_000093.1:p.Phe417Leu