Canonical Allele Identifier: CA2610724528

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835215-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835215G>T , CM000672.2:g.102835215G>T	GRCh38
NC_000010.10:g.104594972G>T , CM000672.1:g.104594972G>T	GRCh37
NC_000010.9:g.104584962G>T	NCBI36
NG_007955.1:g.7319C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+39C>A MANE Select	ENSP00000358903.3:n.436+39C>A
ENST00000638190.1:c.436+39C>A	ENSP00000492539.1:n.436+39C>A
ENST00000638272.1:c.297+1850C>A	ENSP00000491508.1:n.297+1850C>A
ENST00000638971.1:c.436+39C>A	ENSP00000492313.1:n.436+39C>A
ENST00000639393.1:c.436+39C>A	ENSP00000492651.1:n.436+39C>A
ENST00000640633.1:n.198+39C>A
ENST00000369887.3:c.436+39C>A	ENSP00000358903.3:n.436+39C>A
ENST00000489268.1:n.690+39C>A
NM_000102.3:c.436+39C>A	NP_000093.1:n.436+39C>A
NM_000102.4:c.436+39C>A MANE Select	NP_000093.1:n.436+39C>A