Canonical Allele Identifier: CA471287383

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590696T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830939T>C , CM000672.2:g.102830939T>C	GRCh38
NC_000010.10:g.104590696T>C , CM000672.1:g.104590696T>C	GRCh37
NC_000010.9:g.104580686T>C	NCBI36
NG_007955.1:g.11595A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1290A>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Val430=
ENST00000638190.1:c.987A>G (CYP17A1)	ENSP00000492539.1:p.Val329=
ENST00000638272.1:c.834A>G (CYP17A1)	ENSP00000491508.1:p.Val278=
ENST00000638971.1:c.1203A>G (CYP17A1)	ENSP00000492313.1:p.Val401=
ENST00000639393.1:c.1293A>G (CYP17A1)	ENSP00000492651.1:p.Val431=
ENST00000640633.1:n.1052A>G (CYP17A1)
ENST00000647664.1:c.*621T>C (WBP1L)	ENSP00000498131.1:n.*621T>C
ENST00000369887.3:c.1290A>G (CYP17A1)	ENSP00000358903.3:p.Val430=
NM_000102.3:c.1290A>G (CYP17A1)	NP_000093.1:p.Val430=
NM_000102.4:c.1290A>G (CYP17A1) MANE Select	NP_000093.1:p.Val430=