Canonical Allele Identifier: CA1932840731

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844166728
• gnomAD v4: 10-102836665-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102836665A>G , CM000672.2:g.102836665A>G	GRCh38
NC_000010.10:g.104596422A>G , CM000672.1:g.104596422A>G	GRCh37
NC_000010.9:g.104586412A>G	NCBI36
NG_007955.1:g.5869T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.297+400T>C MANE Select	ENSP00000358903.3:n.297+400T>C
ENST00000638190.1:c.297+400T>C	ENSP00000492539.1:n.297+400T>C
ENST00000638272.1:c.297+400T>C	ENSP00000491508.1:n.297+400T>C
ENST00000638971.1:c.297+400T>C	ENSP00000492313.1:n.297+400T>C
ENST00000639393.1:c.297+400T>C	ENSP00000492651.1:n.297+400T>C
ENST00000640633.1:n.59+49T>C
ENST00000369887.3:c.297+400T>C	ENSP00000358903.3:n.297+400T>C
ENST00000489268.1:n.350+400T>C
NM_000102.3:c.297+400T>C	NP_000093.1:n.297+400T>C
NM_000102.4:c.297+400T>C MANE Select	NP_000093.1:n.297+400T>C