Canonical Allele Identifier: CA471298339

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1234235286
• MyVariant Identifiers: chr10:g.104595068G>A (hg19) ; chr10:g.102835311G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835311G>A , CM000672.2:g.102835311G>A	GRCh38
NC_000010.10:g.104595068G>A , CM000672.1:g.104595068G>A	GRCh37
NC_000010.9:g.104585058G>A	NCBI36
NG_007955.1:g.7223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.379C>T MANE Select	ENSP00000358903.3:p.Leu127=
ENST00000638190.1:c.379C>T	ENSP00000492539.1:p.Leu127=
ENST00000638272.1:c.297+1754C>T	ENSP00000491508.1:n.297+1754C>T
ENST00000638971.1:c.379C>T	ENSP00000492313.1:p.Leu127=
ENST00000639393.1:c.379C>T	ENSP00000492651.1:p.Leu127=
ENST00000640633.1:n.141C>T
ENST00000369887.3:c.379C>T	ENSP00000358903.3:p.Leu127=
ENST00000489268.1:n.633C>T
NM_000102.3:c.379C>T	NP_000093.1:p.Leu127=
NM_000102.4:c.379C>T MANE Select	NP_000093.1:p.Leu127=