Canonical Allele Identifier: CA931952943

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844145006
• gnomAD v3: 10-102835191-CCT-C
• gnomAD v4: 10-102835191-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835195_102835196del , CM000672.2:g.102835195_102835196del	GRCh38
NC_000010.10:g.104594952_104594953del , CM000672.1:g.104594952_104594953del	GRCh37
NC_000010.9:g.104584942_104584943del	NCBI36
NG_007955.1:g.7341_7342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+61_436+62del MANE Select	ENSP00000358903.3:n.436+61_436+62del
ENST00000638190.1:c.436+61_436+62del	ENSP00000492539.1:n.436+61_436+62del
ENST00000638272.1:c.297+1872_297+1873del	ENSP00000491508.1:n.297+1872_297+1873del
ENST00000638971.1:c.436+61_436+62del	ENSP00000492313.1:n.436+61_436+62del
ENST00000639393.1:c.436+61_436+62del	ENSP00000492651.1:n.436+61_436+62del
ENST00000640633.1:n.198+61_198+62del
ENST00000369887.3:c.436+61_436+62del	ENSP00000358903.3:n.436+61_436+62del
ENST00000489268.1:n.690+61_690+62del
NM_000102.3:c.436+61_436+62del	NP_000093.1:n.436+61_436+62del
NM_000102.4:c.436+61_436+62del MANE Select	NP_000093.1:n.436+61_436+62del