Canonical Allele Identifier: CA1932867252
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830958_102830959delinsTG , CM000672.2:g.102830958_102830959delinsTG GRCh38
NC_000010.10:g.104590715_104590716delinsTG , CM000672.1:g.104590715_104590716delinsTG GRCh37
NC_000010.9:g.104580705_104580706delinsTG NCBI36
NG_007955.1:g.11575_11576delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1270_1271delinsCA (CYP17A1) MANE Select ENSP00000358903.3:p.Gln424=
ENST00000638190.1:c.967_968delinsCA (CYP17A1) ENSP00000492539.1:p.Gln323=
ENST00000638272.1:c.814_815delinsCA (CYP17A1) ENSP00000491508.1:p.Gln272=
ENST00000638971.1:c.1183_1184delinsCA (CYP17A1) ENSP00000492313.1:p.Gln395=
ENST00000639393.1:c.1273_1274delinsCA (CYP17A1) ENSP00000492651.1:p.Gln425=
ENST00000640633.1:n.1032_1033delinsCA (CYP17A1)
ENST00000647664.1:c.*628+12_*628+13delinsTG (WBP1L) ENSP00000498131.1:n.*628+12_*628+13delinsTG
ENST00000369887.3:c.1270_1271delinsCA (CYP17A1) ENSP00000358903.3:p.Gln424=
ENST00000469683.1:n.223_224delinsCA (CYP17A1)
NM_000102.3:c.1270_1271delinsCA (CYP17A1) NP_000093.1:p.Gln424=
NM_000102.4:c.1270_1271delinsCA (CYP17A1) MANE Select NP_000093.1:p.Gln424=