Canonical Allele Identifier: CA931952911
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1844143955
gnomAD v3: 10-102835162-A-G
gnomAD v4: 10-102835162-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835162A>G , CM000672.2:g.102835162A>G GRCh38
NC_000010.10:g.104594919A>G , CM000672.1:g.104594919A>G GRCh37
NC_000010.9:g.104584909A>G NCBI36
NG_007955.1:g.7372T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.436+92T>C MANE Select ENSP00000358903.3:n.436+92T>C
ENST00000638190.1:c.436+92T>C ENSP00000492539.1:n.436+92T>C
ENST00000638272.1:c.297+1903T>C ENSP00000491508.1:n.297+1903T>C
ENST00000638971.1:c.436+92T>C ENSP00000492313.1:n.436+92T>C
ENST00000639393.1:c.436+92T>C ENSP00000492651.1:n.436+92T>C
ENST00000640633.1:n.198+92T>C
ENST00000369887.3:c.436+92T>C ENSP00000358903.3:n.436+92T>C
ENST00000489268.1:n.690+92T>C
NM_000102.3:c.436+92T>C NP_000093.1:n.436+92T>C
NM_000102.4:c.436+92T>C MANE Select NP_000093.1:n.436+92T>C
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