Canonical Allele Identifier: CA2574654680
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831010del , CM000672.2:g.102831010del GRCh38
NC_000010.10:g.104590767del , CM000672.1:g.104590767del GRCh37
NC_000010.9:g.104580757del NCBI36
NG_007955.1:g.11525del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1244-24del (CYP17A1) MANE Select ENSP00000358903.3:n.1244-24del
ENST00000638190.1:c.941-24del (CYP17A1) ENSP00000492539.1:n.941-24del
ENST00000638272.1:c.788-24del (CYP17A1) ENSP00000491508.1:n.788-24del
ENST00000638971.1:c.1157-24del (CYP17A1) ENSP00000492313.1:n.1157-24del
ENST00000639393.1:c.1247-24del (CYP17A1) ENSP00000492651.1:n.1247-24del
ENST00000640633.1:n.1006-24del (CYP17A1)
ENST00000647664.1:c.*628+64del (WBP1L) ENSP00000498131.1:n.*628+64del
ENST00000369887.3:c.1244-24del (CYP17A1) ENSP00000358903.3:n.1244-24del
ENST00000469683.1:n.197-24del (CYP17A1)
NM_000102.3:c.1244-24del (CYP17A1) NP_000093.1:n.1244-24del
NM_000102.4:c.1244-24del (CYP17A1) MANE Select NP_000093.1:n.1244-24del