Canonical Allele Identifier: CA931952965

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844145566
• gnomAD v3: 10-102835223-C-A
• gnomAD v4: 10-102835223-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835223C>A , CM000672.2:g.102835223C>A	GRCh38
NC_000010.10:g.104594980C>A , CM000672.1:g.104594980C>A	GRCh37
NC_000010.9:g.104584970C>A	NCBI36
NG_007955.1:g.7311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+31G>T MANE Select	ENSP00000358903.3:n.436+31G>T
ENST00000638190.1:c.436+31G>T	ENSP00000492539.1:n.436+31G>T
ENST00000638272.1:c.297+1842G>T	ENSP00000491508.1:n.297+1842G>T
ENST00000638971.1:c.436+31G>T	ENSP00000492313.1:n.436+31G>T
ENST00000639393.1:c.436+31G>T	ENSP00000492651.1:n.436+31G>T
ENST00000640633.1:n.198+31G>T
ENST00000369887.3:c.436+31G>T	ENSP00000358903.3:n.436+31G>T
ENST00000489268.1:n.690+31G>T
NM_000102.3:c.436+31G>T	NP_000093.1:n.436+31G>T
NM_000102.4:c.436+31G>T MANE Select	NP_000093.1:n.436+31G>T