Canonical Allele Identifier: CA2574654671

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830853_102830855del , CM000672.2:g.102830853_102830855del	GRCh38
NC_000010.10:g.104590610_104590612del , CM000672.1:g.104590610_104590612del	GRCh37
NC_000010.9:g.104580600_104580602del	NCBI36
NG_007955.1:g.11684_11686del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1379_1381del (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu460del
ENST00000638190.1:c.1076_1078del (CYP17A1)	ENSP00000492539.1:p.Leu359del
ENST00000638272.1:c.923_925del (CYP17A1)	ENSP00000491508.1:p.Leu308del
ENST00000638971.1:c.1292_1294del (CYP17A1)	ENSP00000492313.1:p.Leu431del
ENST00000639393.1:c.1382_1384del (CYP17A1)	ENSP00000492651.1:p.Leu461del
ENST00000640633.1:n.1141_1143del (CYP17A1)
ENST00000647664.1:c.*535_*537del (WBP1L)	ENSP00000498131.1:n.*535_*537del
ENST00000369887.3:c.1379_1381del (CYP17A1)	ENSP00000358903.3:p.Leu460del
NM_000102.3:c.1379_1381del (CYP17A1)	NP_000093.1:p.Leu460del
NM_000102.4:c.1379_1381del (CYP17A1) MANE Select	NP_000093.1:p.Leu460del