Canonical Allele Identifier: CA595636620

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1193179062
• gnomAD v2: 10-104596782-G-T
• gnomAD v4: 10-102837025-G-T
• MyVariant Identifiers: chr10:g.104596782G>T (hg19) ; chr10:g.102837025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837025G>T , CM000672.2:g.102837025G>T	GRCh38
NC_000010.10:g.104596782G>T , CM000672.1:g.104596782G>T	GRCh37
NC_000010.9:g.104586772G>T	NCBI36
NG_007955.1:g.5509C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.297+40C>A MANE Select	ENSP00000358903.3:n.297+40C>A
ENST00000638190.1:c.297+40C>A	ENSP00000492539.1:n.297+40C>A
ENST00000638272.1:c.297+40C>A	ENSP00000491508.1:n.297+40C>A
ENST00000638971.1:c.297+40C>A	ENSP00000492313.1:n.297+40C>A
ENST00000639393.1:c.297+40C>A	ENSP00000492651.1:n.297+40C>A
ENST00000369887.3:c.297+40C>A	ENSP00000358903.3:n.297+40C>A
ENST00000489268.1:n.350+40C>A
NM_000102.3:c.297+40C>A	NP_000093.1:n.297+40C>A
NM_000102.4:c.297+40C>A MANE Select	NP_000093.1:n.297+40C>A