Canonical Allele Identifier: CA1932868190

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831365_102831367delinsAGG , CM000672.2:g.102831365_102831367delinsAGG	GRCh38
NC_000010.10:g.104591122_104591124delinsAGG , CM000672.1:g.104591122_104591124delinsAGG	GRCh37
NC_000010.9:g.104581112_104581114delinsAGG	NCBI36
NG_007955.1:g.11167_11169delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1243+141_1243+143delinsCCT (CYP17A1) MANE Select	ENSP00000358903.3:n.1243+141_1243+143delinsCCT
ENST00000638190.1:c.940+141_940+143delinsCCT (CYP17A1)	ENSP00000492539.1:n.940+141_940+143delinsCCT
ENST00000638272.1:c.787+141_787+143delinsCCT (CYP17A1)	ENSP00000491508.1:n.787+141_787+143delinsCCT
ENST00000638971.1:c.1156+141_1156+143delinsCCT (CYP17A1)	ENSP00000492313.1:n.1156+141_1156+143delinsCCT
ENST00000639393.1:c.1246+141_1246+143delinsCCT (CYP17A1)	ENSP00000492651.1:n.1246+141_1246+143delinsCCT
ENST00000640633.1:n.1005+141_1005+143delinsCCT (CYP17A1)
ENST00000647664.1:c.*629-233_*629-231delinsAGG (WBP1L)	ENSP00000498131.1:n.*629-233_*629-231delinsAGG
ENST00000369887.3:c.1243+141_1243+143delinsCCT (CYP17A1)	ENSP00000358903.3:n.1243+141_1243+143delinsCCT
ENST00000469683.1:n.196+141_196+143delinsCCT (CYP17A1)
NM_000102.3:c.1243+141_1243+143delinsCCT (CYP17A1)	NP_000093.1:n.1243+141_1243+143delinsCCT
NM_000102.4:c.1243+141_1243+143delinsCCT (CYP17A1) MANE Select	NP_000093.1:n.1243+141_1243+143delinsCCT