Canonical Allele Identifier: CA2610724438

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835129-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835129A>G , CM000672.2:g.102835129A>G	GRCh38
NC_000010.10:g.104594886A>G , CM000672.1:g.104594886A>G	GRCh37
NC_000010.9:g.104584876A>G	NCBI36
NG_007955.1:g.7405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-115T>C MANE Select	ENSP00000358903.3:n.437-115T>C
ENST00000638190.1:c.437-115T>C	ENSP00000492539.1:n.437-115T>C
ENST00000638272.1:c.298-1921T>C	ENSP00000491508.1:n.298-1921T>C
ENST00000638971.1:c.437-115T>C	ENSP00000492313.1:n.437-115T>C
ENST00000639393.1:c.437-115T>C	ENSP00000492651.1:n.437-115T>C
ENST00000640633.1:n.199-115T>C
ENST00000369887.3:c.437-115T>C	ENSP00000358903.3:n.437-115T>C
ENST00000489268.1:n.691-115T>C
NM_000102.3:c.437-115T>C	NP_000093.1:n.437-115T>C
NM_000102.4:c.437-115T>C MANE Select	NP_000093.1:n.437-115T>C