Canonical Allele Identifier: CA377939721

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102834784-C-G
• MyVariant Identifiers: chr10:g.104594541C>G (hg19) ; chr10:g.102834784C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834784C>G , CM000672.2:g.102834784C>G	GRCh38
NC_000010.10:g.104594541C>G , CM000672.1:g.104594541C>G	GRCh37
NC_000010.9:g.104584531C>G	NCBI36
NG_007955.1:g.7750G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.666+1G>C MANE Select	ENSP00000358903.3:n.666+1G>C
ENST00000638190.1:c.666+1G>C	ENSP00000492539.1:n.666+1G>C
ENST00000638272.1:c.298-1576G>C	ENSP00000491508.1:n.298-1576G>C
ENST00000638971.1:c.666+1G>C	ENSP00000492313.1:n.666+1G>C
ENST00000639393.1:c.666+1G>C	ENSP00000492651.1:n.666+1G>C
ENST00000640633.1:n.428+1G>C
ENST00000369887.3:c.666+1G>C	ENSP00000358903.3:n.666+1G>C
ENST00000489268.1:n.921G>C
NM_000102.3:c.666+1G>C	NP_000093.1:n.666+1G>C
NM_000102.4:c.666+1G>C MANE Select	NP_000093.1:n.666+1G>C