Canonical Allele Identifier: CA2610725127

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102836725-C-CCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836725_102836726insCGG , CM000672.2:g.102836725_102836726insCGG	GRCh38
NC_000010.10:g.104596482_104596483insCGG , CM000672.1:g.104596482_104596483insCGG	GRCh37
NC_000010.9:g.104586472_104586473insCGG	NCBI36
NG_007955.1:g.5808_5809insCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+339_297+340insCCG MANE Select	ENSP00000358903.3:n.297+339_297+340insCCG
ENST00000638190.1:c.297+339_297+340insCCG	ENSP00000492539.1:n.297+339_297+340insCCG
ENST00000638272.1:c.297+339_297+340insCCG	ENSP00000491508.1:n.297+339_297+340insCCG
ENST00000638971.1:c.297+339_297+340insCCG	ENSP00000492313.1:n.297+339_297+340insCCG
ENST00000639393.1:c.297+339_297+340insCCG	ENSP00000492651.1:n.297+339_297+340insCCG
ENST00000640633.1:n.47_48insCCG
ENST00000369887.3:c.297+339_297+340insCCG	ENSP00000358903.3:n.297+339_297+340insCCG
ENST00000489268.1:n.350+339_350+340insCCG
NM_000102.3:c.297+339_297+340insCCG	NP_000093.1:n.297+339_297+340insCCG
NM_000102.4:c.297+339_297+340insCCG MANE Select	NP_000093.1:n.297+339_297+340insCCG