Canonical Allele Identifier: CA2610724449

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835135-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835135A>G , CM000672.2:g.102835135A>G	GRCh38
NC_000010.10:g.104594892A>G , CM000672.1:g.104594892A>G	GRCh37
NC_000010.9:g.104584882A>G	NCBI36
NG_007955.1:g.7399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+119T>C MANE Select	ENSP00000358903.3:n.436+119T>C
ENST00000638190.1:c.436+119T>C	ENSP00000492539.1:n.436+119T>C
ENST00000638272.1:c.298-1927T>C	ENSP00000491508.1:n.298-1927T>C
ENST00000638971.1:c.436+119T>C	ENSP00000492313.1:n.436+119T>C
ENST00000639393.1:c.436+119T>C	ENSP00000492651.1:n.436+119T>C
ENST00000640633.1:n.198+119T>C
ENST00000369887.3:c.436+119T>C	ENSP00000358903.3:n.436+119T>C
ENST00000489268.1:n.690+119T>C
NM_000102.3:c.436+119T>C	NP_000093.1:n.436+119T>C
NM_000102.4:c.436+119T>C MANE Select	NP_000093.1:n.436+119T>C