Canonical Allele Identifier: CA595636771

Gene: CYP17A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835179del , CM000672.2:g.102835179del	GRCh38
NC_000010.10:g.104594936del , CM000672.1:g.104594936del	GRCh37
NC_000010.9:g.104584926del	NCBI36
NG_007955.1:g.7358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+78del MANE Select	ENSP00000358903.3:n.436+78del
ENST00000638190.1:c.436+78del	ENSP00000492539.1:n.436+78del
ENST00000638272.1:c.297+1889del	ENSP00000491508.1:n.297+1889del
ENST00000638971.1:c.436+78del	ENSP00000492313.1:n.436+78del
ENST00000639393.1:c.436+78del	ENSP00000492651.1:n.436+78del
ENST00000640633.1:n.198+78del
ENST00000369887.3:c.436+78del	ENSP00000358903.3:n.436+78del
ENST00000489268.1:n.690+78del
NM_000102.3:c.436+78del	NP_000093.1:n.436+78del
NM_000102.4:c.436+78del MANE Select	NP_000093.1:n.436+78del