Canonical Allele Identifier: CA377940318
Gene: CYP17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-102835285-G-C
MyVariant Identifiers: chr10:g.104595042G>C (hg19) chr10:g.102835285G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835285G>C , CM000672.2:g.102835285G>C GRCh38
NC_000010.10:g.104595042G>C , CM000672.1:g.104595042G>C GRCh37
NC_000010.9:g.104585032G>C NCBI36
NG_007955.1:g.7249C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.405C>G MANE Select ENSP00000358903.3:p.Phe135Leu
ENST00000638190.1:c.405C>G ENSP00000492539.1:p.Phe135Leu
ENST00000638272.1:c.297+1780C>G ENSP00000491508.1:n.297+1780C>G
ENST00000638971.1:c.405C>G ENSP00000492313.1:p.Phe135Leu
ENST00000639393.1:c.405C>G ENSP00000492651.1:p.Phe135Leu
ENST00000640633.1:n.167C>G
ENST00000369887.3:c.405C>G ENSP00000358903.3:p.Phe135Leu
ENST00000489268.1:n.659C>G
NM_000102.3:c.405C>G NP_000093.1:p.Phe135Leu
NM_000102.4:c.405C>G MANE Select NP_000093.1:p.Phe135Leu
Search 100 bp 5'
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