Canonical Allele Identifier: CA1932876629

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844142866
• gnomAD v4: 10-102835096-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835101dup , CM000672.2:g.102835101dup	GRCh38
NC_000010.10:g.104594858dup , CM000672.1:g.104594858dup	GRCh37
NC_000010.9:g.104584848dup	NCBI36
NG_007955.1:g.7437dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-83dup MANE Select	ENSP00000358903.3:n.437-83dup
ENST00000638190.1:c.437-83dup	ENSP00000492539.1:n.437-83dup
ENST00000638272.1:c.298-1889dup	ENSP00000491508.1:n.298-1889dup
ENST00000638971.1:c.437-83dup	ENSP00000492313.1:n.437-83dup
ENST00000639393.1:c.437-83dup	ENSP00000492651.1:n.437-83dup
ENST00000640633.1:n.199-83dup
ENST00000369887.3:c.437-83dup	ENSP00000358903.3:n.437-83dup
ENST00000489268.1:n.691-83dup
NM_000102.3:c.437-83dup	NP_000093.1:n.437-83dup
NM_000102.4:c.437-83dup MANE Select	NP_000093.1:n.437-83dup