Canonical Allele Identifier: CA212294381

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1038978276
• gnomAD v4: 10-102835224-C-A
• MyVariant Identifiers: chr10:g.104594981C>A (hg19) ; chr10:g.102835224C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835224C>A , CM000672.2:g.102835224C>A	GRCh38
NC_000010.10:g.104594981C>A , CM000672.1:g.104594981C>A	GRCh37
NC_000010.9:g.104584971C>A	NCBI36
NG_007955.1:g.7310G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.436+30G>T MANE Select	ENSP00000358903.3:n.436+30G>T
ENST00000638190.1:c.436+30G>T	ENSP00000492539.1:n.436+30G>T
ENST00000638272.1:c.297+1841G>T	ENSP00000491508.1:n.297+1841G>T
ENST00000638971.1:c.436+30G>T	ENSP00000492313.1:n.436+30G>T
ENST00000639393.1:c.436+30G>T	ENSP00000492651.1:n.436+30G>T
ENST00000640633.1:n.198+30G>T
ENST00000369887.3:c.436+30G>T	ENSP00000358903.3:n.436+30G>T
ENST00000489268.1:n.690+30G>T
NM_000102.3:c.436+30G>T	NP_000093.1:n.436+30G>T
NM_000102.4:c.436+30G>T MANE Select	NP_000093.1:n.436+30G>T