Canonical Allele Identifier: CA5669554

Gene: CYP17A1

Linked Data

• dbSNP Id: rs752593169
• ExAC: 10:104594796 TGGGAAA / T
• MyVariant Identifiers: chr10:g.104594797_104594802del (hg19) ; chr10:g.102835040_102835045del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835040_102835045del , CM000672.2:g.102835040_102835045del	GRCh38
NC_000010.10:g.104594797_104594802del , CM000672.1:g.104594797_104594802del	GRCh37
NC_000010.9:g.104584787_104584792del	NCBI36
NG_007955.1:g.7489_7494del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-31_437-26del MANE Select	ENSP00000358903.3:n.437-31_437-26del
ENST00000638190.1:c.437-31_437-26del	ENSP00000492539.1:n.437-31_437-26del
ENST00000638272.1:c.298-1837_298-1832del	ENSP00000491508.1:n.298-1837_298-1832del
ENST00000638971.1:c.437-31_437-26del	ENSP00000492313.1:n.437-31_437-26del
ENST00000639393.1:c.437-31_437-26del	ENSP00000492651.1:n.437-31_437-26del
ENST00000640633.1:n.199-31_199-26del
ENST00000369887.3:c.437-31_437-26del	ENSP00000358903.3:n.437-31_437-26del
ENST00000489268.1:n.691-31_691-26del
NM_000102.3:c.437-31_437-26del	NP_000093.1:n.437-31_437-26del
NM_000102.4:c.437-31_437-26del MANE Select	NP_000093.1:n.437-31_437-26del