Canonical Allele Identifier: CA931964127

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1844081953
• gnomAD v3: 10-102831087-CTGAT-C
• gnomAD v4: 10-102831087-CTGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831088_102831091del , CM000672.2:g.102831088_102831091del	GRCh38
NC_000010.10:g.104590845_104590848del , CM000672.1:g.104590845_104590848del	GRCh37
NC_000010.9:g.104580835_104580838del	NCBI36
NG_007955.1:g.11443_11446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1244-106_1244-103del (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-106_1244-103del
ENST00000638190.1:c.941-106_941-103del (CYP17A1)	ENSP00000492539.1:n.941-106_941-103del
ENST00000638272.1:c.788-106_788-103del (CYP17A1)	ENSP00000491508.1:n.788-106_788-103del
ENST00000638971.1:c.1157-106_1157-103del (CYP17A1)	ENSP00000492313.1:n.1157-106_1157-103del
ENST00000639393.1:c.1247-106_1247-103del (CYP17A1)	ENSP00000492651.1:n.1247-106_1247-103del
ENST00000640633.1:n.1006-106_1006-103del (CYP17A1)
ENST00000647664.1:c.*628+142_*628+145del (WBP1L)	ENSP00000498131.1:n.*628+142_*628+145del
ENST00000369887.3:c.1244-106_1244-103del (CYP17A1)	ENSP00000358903.3:n.1244-106_1244-103del
ENST00000469683.1:n.197-106_197-103del (CYP17A1)
NM_000102.3:c.1244-106_1244-103del (CYP17A1)	NP_000093.1:n.1244-106_1244-103del
NM_000102.4:c.1244-106_1244-103del (CYP17A1) MANE Select	NP_000093.1:n.1244-106_1244-103del