Canonical Allele Identifier: CA2574654710
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831615C>G , CM000672.2:g.102831615C>G GRCh38
NC_000010.10:g.104591372C>G , CM000672.1:g.104591372C>G GRCh37
NC_000010.9:g.104581362C>G NCBI36
NG_007955.1:g.10919G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1140-4G>C (CYP17A1) MANE Select ENSP00000358903.3:n.1140-4G>C
ENST00000638190.1:c.837-4G>C (CYP17A1) ENSP00000492539.1:n.837-4G>C
ENST00000638272.1:c.684-4G>C (CYP17A1) ENSP00000491508.1:n.684-4G>C
ENST00000638971.1:c.1053-4G>C (CYP17A1) ENSP00000492313.1:n.1053-4G>C
ENST00000639393.1:c.1140-1G>C (CYP17A1) ENSP00000492651.1:n.1140-1G>C
ENST00000640633.1:n.902-4G>C (CYP17A1)
ENST00000647664.1:c.*646C>G (WBP1L) ENSP00000498131.1:n.*646C>G
ENST00000369887.3:c.1140-4G>C (CYP17A1) ENSP00000358903.3:n.1140-4G>C
ENST00000469683.1:n.89G>C (CYP17A1)
NM_000102.3:c.1140-4G>C (CYP17A1) NP_000093.1:n.1140-4G>C
NM_000102.4:c.1140-4G>C (CYP17A1) MANE Select NP_000093.1:n.1140-4G>C