Canonical Allele Identifier: CA2610725308

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102836844-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836845dup , CM000672.2:g.102836845dup	GRCh38
NC_000010.10:g.104596602dup , CM000672.1:g.104596602dup	GRCh37
NC_000010.9:g.104586592dup	NCBI36
NG_007955.1:g.5689dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.297+220dup MANE Select	ENSP00000358903.3:n.297+220dup
ENST00000638190.1:c.297+220dup	ENSP00000492539.1:n.297+220dup
ENST00000638272.1:c.297+220dup	ENSP00000491508.1:n.297+220dup
ENST00000638971.1:c.297+220dup	ENSP00000492313.1:n.297+220dup
ENST00000639393.1:c.297+220dup	ENSP00000492651.1:n.297+220dup
ENST00000369887.3:c.297+220dup	ENSP00000358903.3:n.297+220dup
ENST00000489268.1:n.350+220dup
NM_000102.3:c.297+220dup	NP_000093.1:n.297+220dup
NM_000102.4:c.297+220dup MANE Select	NP_000093.1:n.297+220dup