Canonical Allele Identifier: CA212294258

Gene: CYP17A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835108A>T , CM000672.2:g.102835108A>T	GRCh38
NC_000010.10:g.104594865A>T , CM000672.1:g.104594865A>T	GRCh37
NC_000010.9:g.104584855A>T	NCBI36
NG_007955.1:g.7426T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-94T>A MANE Select	ENSP00000358903.3:n.437-94T>A
ENST00000638190.1:c.437-94T>A	ENSP00000492539.1:n.437-94T>A
ENST00000638272.1:c.298-1900T>A	ENSP00000491508.1:n.298-1900T>A
ENST00000638971.1:c.437-94T>A	ENSP00000492313.1:n.437-94T>A
ENST00000639393.1:c.437-94T>A	ENSP00000492651.1:n.437-94T>A
ENST00000640633.1:n.199-94T>A
ENST00000369887.3:c.437-94T>A	ENSP00000358903.3:n.437-94T>A
ENST00000489268.1:n.691-94T>A
NM_000102.3:c.437-94T>A	NP_000093.1:n.437-94T>A
NM_000102.4:c.437-94T>A MANE Select	NP_000093.1:n.437-94T>A