Canonical Allele Identifier: CA659059408

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1396981926
• gnomAD v3: 10-102835107-TAGC-T
• gnomAD v4: 10-102835107-TAGC-T
• MyVariant Identifiers: chr10:g.104594865_104594867del (hg19) ; chr10:g.102835108_102835110del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835110_102835112del , CM000672.2:g.102835110_102835112del	GRCh38
NC_000010.10:g.104594867_104594869del , CM000672.1:g.104594867_104594869del	GRCh37
NC_000010.9:g.104584857_104584859del	NCBI36
NG_007955.1:g.7424_7426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-96_437-94del MANE Select	ENSP00000358903.3:n.437-96_437-94del
ENST00000638190.1:c.437-96_437-94del	ENSP00000492539.1:n.437-96_437-94del
ENST00000638272.1:c.298-1902_298-1900del	ENSP00000491508.1:n.298-1902_298-1900del
ENST00000638971.1:c.437-96_437-94del	ENSP00000492313.1:n.437-96_437-94del
ENST00000639393.1:c.437-96_437-94del	ENSP00000492651.1:n.437-96_437-94del
ENST00000640633.1:n.199-96_199-94del
ENST00000369887.3:c.437-96_437-94del	ENSP00000358903.3:n.437-96_437-94del
ENST00000489268.1:n.691-96_691-94del
NM_000102.3:c.437-96_437-94del	NP_000093.1:n.437-96_437-94del
NM_000102.4:c.437-96_437-94del MANE Select	NP_000093.1:n.437-96_437-94del