Canonical Allele Identifier: CA2610721287

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102831084-ACCCTGATCTGAGGATGTAGCCTTATTATGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831085_102831114del , CM000672.2:g.102831085_102831114del	GRCh38
NC_000010.10:g.104590842_104590871del , CM000672.1:g.104590842_104590871del	GRCh37
NC_000010.9:g.104580832_104580861del	NCBI36
NG_007955.1:g.11420_11449del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1244-129_1244-100del (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-129_1244-100del
ENST00000638190.1:c.941-129_941-100del (CYP17A1)	ENSP00000492539.1:n.941-129_941-100del
ENST00000638272.1:c.788-129_788-100del (CYP17A1)	ENSP00000491508.1:n.788-129_788-100del
ENST00000638971.1:c.1157-129_1157-100del (CYP17A1)	ENSP00000492313.1:n.1157-129_1157-100del
ENST00000639393.1:c.1247-129_1247-100del (CYP17A1)	ENSP00000492651.1:n.1247-129_1247-100del
ENST00000640633.1:n.1006-129_1006-100del (CYP17A1)
ENST00000647664.1:c.*628+139_*628+168del (WBP1L)	ENSP00000498131.1:n.*628+139_*628+168del
ENST00000369887.3:c.1244-129_1244-100del (CYP17A1)	ENSP00000358903.3:n.1244-129_1244-100del
ENST00000469683.1:n.197-129_197-100del (CYP17A1)
NM_000102.3:c.1244-129_1244-100del (CYP17A1)	NP_000093.1:n.1244-129_1244-100del
NM_000102.4:c.1244-129_1244-100del (CYP17A1) MANE Select	NP_000093.1:n.1244-129_1244-100del