Canonical Allele Identifier: CA377938389

Gene: CYP17A1 WBP1L

Linked Data

• ClinVar Variation Id: 2681105
• ClinVar RCV Id: RCV003468640
• MyVariant Identifiers: chr10:g.104590743C>G (hg19) ; chr10:g.102830986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830986C>G , CM000672.2:g.102830986C>G	GRCh38
NC_000010.10:g.104590743C>G , CM000672.1:g.104590743C>G	GRCh37
NC_000010.9:g.104580733C>G	NCBI36
NG_007955.1:g.11548G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1244-1G>C (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-1G>C
ENST00000638190.1:c.941-1G>C (CYP17A1)	ENSP00000492539.1:n.941-1G>C
ENST00000638272.1:c.788-1G>C (CYP17A1)	ENSP00000491508.1:n.788-1G>C
ENST00000638971.1:c.1157-1G>C (CYP17A1)	ENSP00000492313.1:n.1157-1G>C
ENST00000639393.1:c.1247-1G>C (CYP17A1)	ENSP00000492651.1:n.1247-1G>C
ENST00000640633.1:n.1006-1G>C (CYP17A1)
ENST00000647664.1:c.*628+40C>G (WBP1L)	ENSP00000498131.1:n.*628+40C>G
ENST00000369887.3:c.1244-1G>C (CYP17A1)	ENSP00000358903.3:n.1244-1G>C
ENST00000469683.1:n.197-1G>C (CYP17A1)
NM_000102.3:c.1244-1G>C (CYP17A1)	NP_000093.1:n.1244-1G>C
NM_000102.4:c.1244-1G>C (CYP17A1) MANE Select	NP_000093.1:n.1244-1G>C