Canonical Allele Identifier: CA2610723912

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833894-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833895_102833896del , CM000672.2:g.102833895_102833896del	GRCh38
NC_000010.10:g.104593652_104593653del , CM000672.1:g.104593652_104593653del	GRCh37
NC_000010.9:g.104583642_104583643del	NCBI36
NG_007955.1:g.8638_8639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-282_152-281del
ENST00000369887.4:c.753+140_753+141del (CYP17A1) MANE Select	ENSP00000358903.3:n.753+140_753+141del
ENST00000638190.1:c.666+889_666+890del (CYP17A1)	ENSP00000492539.1:n.666+889_666+890del
ENST00000638272.1:c.298-688_298-687del (CYP17A1)	ENSP00000491508.1:n.298-688_298-687del
ENST00000638971.1:c.667-688_667-687del (CYP17A1)	ENSP00000492313.1:n.667-688_667-687del
ENST00000639393.1:c.753+140_753+141del (CYP17A1)	ENSP00000492651.1:n.753+140_753+141del
ENST00000640633.1:n.515+140_515+141del (CYP17A1)
ENST00000369887.3:c.753+140_753+141del (CYP17A1)	ENSP00000358903.3:n.753+140_753+141del
ENST00000489268.1:n.1809_1810del (CYP17A1)
NM_000102.3:c.753+140_753+141del (CYP17A1)	NP_000093.1:n.753+140_753+141del
XR_428804.1:n.206-282_206-281del (CYP17A1-AS1)
NM_000102.4:c.753+140_753+141del (CYP17A1) MANE Select	NP_000093.1:n.753+140_753+141del