Canonical Allele Identifier: CA2553058541
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831017_102831018insCCC , CM000672.2:g.102831017_102831018insCCC GRCh38
NC_000010.10:g.104590774_104590775insCCC , CM000672.1:g.104590774_104590775insCCC GRCh37
NC_000010.9:g.104580764_104580765insCCC NCBI36
NG_007955.1:g.11516_11517insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1244-33_1244-32insGGG (CYP17A1) MANE Select ENSP00000358903.3:n.1244-33_1244-32insGGG
ENST00000638190.1:c.941-33_941-32insGGG (CYP17A1) ENSP00000492539.1:n.941-33_941-32insGGG
ENST00000638272.1:c.788-33_788-32insGGG (CYP17A1) ENSP00000491508.1:n.788-33_788-32insGGG
ENST00000638971.1:c.1157-33_1157-32insGGG (CYP17A1) ENSP00000492313.1:n.1157-33_1157-32insGGG
ENST00000639393.1:c.1247-33_1247-32insGGG (CYP17A1) ENSP00000492651.1:n.1247-33_1247-32insGGG
ENST00000640633.1:n.1006-33_1006-32insGGG (CYP17A1)
ENST00000647664.1:c.*628+71_*628+72insCCC (WBP1L) ENSP00000498131.1:n.*628+71_*628+72insCCC
ENST00000369887.3:c.1244-33_1244-32insGGG (CYP17A1) ENSP00000358903.3:n.1244-33_1244-32insGGG
ENST00000469683.1:n.197-33_197-32insGGG (CYP17A1)
NM_000102.3:c.1244-33_1244-32insGGG (CYP17A1) NP_000093.1:n.1244-33_1244-32insGGG
NM_000102.4:c.1244-33_1244-32insGGG (CYP17A1) MANE Select NP_000093.1:n.1244-33_1244-32insGGG