Canonical Allele Identifier: CA2610725392

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102836899-CTGGGTGGGGGTCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836900_102836913del , CM000672.2:g.102836900_102836913del	GRCh38
NC_000010.10:g.104596657_104596670del , CM000672.1:g.104596657_104596670del	GRCh37
NC_000010.9:g.104586647_104586660del	NCBI36
NG_007955.1:g.5621_5634del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.297+152_297+165del MANE Select	ENSP00000358903.3:n.297+152_297+165del
ENST00000638190.1:c.297+152_297+165del	ENSP00000492539.1:n.297+152_297+165del
ENST00000638272.1:c.297+152_297+165del	ENSP00000491508.1:n.297+152_297+165del
ENST00000638971.1:c.297+152_297+165del	ENSP00000492313.1:n.297+152_297+165del
ENST00000639393.1:c.297+152_297+165del	ENSP00000492651.1:n.297+152_297+165del
ENST00000369887.3:c.297+152_297+165del	ENSP00000358903.3:n.297+152_297+165del
ENST00000489268.1:n.350+152_350+165del
NM_000102.3:c.297+152_297+165del	NP_000093.1:n.297+152_297+165del
NM_000102.4:c.297+152_297+165del MANE Select	NP_000093.1:n.297+152_297+165del