Canonical Allele Identifier: CA2518540824

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831007_102831008del , CM000672.2:g.102831007_102831008del	GRCh38
NC_000010.10:g.104590764_104590765del , CM000672.1:g.104590764_104590765del	GRCh37
NC_000010.9:g.104580754_104580755del	NCBI36
NG_007955.1:g.11526_11527del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1244-23_1244-22del (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-23_1244-22del
ENST00000638190.1:c.941-23_941-22del (CYP17A1)	ENSP00000492539.1:n.941-23_941-22del
ENST00000638272.1:c.788-23_788-22del (CYP17A1)	ENSP00000491508.1:n.788-23_788-22del
ENST00000638971.1:c.1157-23_1157-22del (CYP17A1)	ENSP00000492313.1:n.1157-23_1157-22del
ENST00000639393.1:c.1247-23_1247-22del (CYP17A1)	ENSP00000492651.1:n.1247-23_1247-22del
ENST00000640633.1:n.1006-23_1006-22del (CYP17A1)
ENST00000647664.1:c.*628+61_*628+62del (WBP1L)	ENSP00000498131.1:n.*628+61_*628+62del
ENST00000369887.3:c.1244-23_1244-22del (CYP17A1)	ENSP00000358903.3:n.1244-23_1244-22del
ENST00000469683.1:n.197-23_197-22del (CYP17A1)
NM_000102.3:c.1244-23_1244-22del (CYP17A1)	NP_000093.1:n.1244-23_1244-22del
NM_000102.4:c.1244-23_1244-22del (CYP17A1) MANE Select	NP_000093.1:n.1244-23_1244-22del