Canonical Allele Identifier: CA2610724383

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835056-C-CCCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835057_102835060dup , CM000672.2:g.102835057_102835060dup	GRCh38
NC_000010.10:g.104594814_104594817dup , CM000672.1:g.104594814_104594817dup	GRCh37
NC_000010.9:g.104584804_104584807dup	NCBI36
NG_007955.1:g.7474_7477dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-46_437-43dup MANE Select	ENSP00000358903.3:n.437-46_437-43dup
ENST00000638190.1:c.437-46_437-43dup	ENSP00000492539.1:n.437-46_437-43dup
ENST00000638272.1:c.298-1852_298-1849dup	ENSP00000491508.1:n.298-1852_298-1849dup
ENST00000638971.1:c.437-46_437-43dup	ENSP00000492313.1:n.437-46_437-43dup
ENST00000639393.1:c.437-46_437-43dup	ENSP00000492651.1:n.437-46_437-43dup
ENST00000640633.1:n.199-46_199-43dup
ENST00000369887.3:c.437-46_437-43dup	ENSP00000358903.3:n.437-46_437-43dup
ENST00000489268.1:n.691-46_691-43dup
NM_000102.3:c.437-46_437-43dup	NP_000093.1:n.437-46_437-43dup
NM_000102.4:c.437-46_437-43dup MANE Select	NP_000093.1:n.437-46_437-43dup