Canonical Allele Identifier: CA377938424
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831518C>G , CM000672.2:g.102831518C>G GRCh38
NC_000010.10:g.104591275C>G , CM000672.1:g.104591275C>G GRCh37
NC_000010.9:g.104581265C>G NCBI36
NG_007955.1:g.11016G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1233G>C (CYP17A1) MANE Select ENSP00000358903.3:p.Gln411His
ENST00000638190.1:c.930G>C (CYP17A1) ENSP00000492539.1:p.Gln310His
ENST00000638272.1:c.777G>C (CYP17A1) ENSP00000491508.1:p.Gln259His
ENST00000638971.1:c.1146G>C (CYP17A1) ENSP00000492313.1:p.Gln382His
ENST00000639393.1:c.1236G>C (CYP17A1) ENSP00000492651.1:p.Gln412His
ENST00000640633.1:n.995G>C (CYP17A1)
ENST00000647664.1:c.*629-80C>G (WBP1L) ENSP00000498131.1:n.*629-80C>G
ENST00000369887.3:c.1233G>C (CYP17A1) ENSP00000358903.3:p.Gln411His
ENST00000469683.1:n.186G>C (CYP17A1)
NM_000102.3:c.1233G>C (CYP17A1) NP_000093.1:p.Gln411His
NM_000102.4:c.1233G>C (CYP17A1) MANE Select NP_000093.1:p.Gln411His