Canonical Allele Identifier: CA5669553

Gene: CYP17A1

Linked Data

• dbSNP Id: rs779250805
• ExAC: 10:104594792 AGG / A
• MyVariant Identifiers: chr10:g.104594793_104594794del (hg19) ; chr10:g.102835036_102835037del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835037_102835038del , CM000672.2:g.102835037_102835038del	GRCh38
NC_000010.10:g.104594794_104594795del , CM000672.1:g.104594794_104594795del	GRCh37
NC_000010.9:g.104584784_104584785del	NCBI36
NG_007955.1:g.7497_7498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-23_437-22del MANE Select	ENSP00000358903.3:n.437-23_437-22del
ENST00000638190.1:c.437-23_437-22del	ENSP00000492539.1:n.437-23_437-22del
ENST00000638272.1:c.298-1829_298-1828del	ENSP00000491508.1:n.298-1829_298-1828del
ENST00000638971.1:c.437-23_437-22del	ENSP00000492313.1:n.437-23_437-22del
ENST00000639393.1:c.437-23_437-22del	ENSP00000492651.1:n.437-23_437-22del
ENST00000640633.1:n.199-23_199-22del
ENST00000369887.3:c.437-23_437-22del	ENSP00000358903.3:n.437-23_437-22del
ENST00000489268.1:n.691-23_691-22del
NM_000102.3:c.437-23_437-22del	NP_000093.1:n.437-23_437-22del
NM_000102.4:c.437-23_437-22del MANE Select	NP_000093.1:n.437-23_437-22del