Canonical Allele Identifier: CA1932876479

Gene: CYP17A1

Linked Data

• dbSNP Id: rs1844142081
• gnomAD v4: 10-102835070-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835072_102835073del , CM000672.2:g.102835072_102835073del	GRCh38
NC_000010.10:g.104594829_104594830del , CM000672.1:g.104594829_104594830del	GRCh37
NC_000010.9:g.104584819_104584820del	NCBI36
NG_007955.1:g.7462_7463del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.437-58_437-57del MANE Select	ENSP00000358903.3:n.437-58_437-57del
ENST00000638190.1:c.437-58_437-57del	ENSP00000492539.1:n.437-58_437-57del
ENST00000638272.1:c.298-1864_298-1863del	ENSP00000491508.1:n.298-1864_298-1863del
ENST00000638971.1:c.437-58_437-57del	ENSP00000492313.1:n.437-58_437-57del
ENST00000639393.1:c.437-58_437-57del	ENSP00000492651.1:n.437-58_437-57del
ENST00000640633.1:n.199-58_199-57del
ENST00000369887.3:c.437-58_437-57del	ENSP00000358903.3:n.437-58_437-57del
ENST00000489268.1:n.691-58_691-57del
NM_000102.3:c.437-58_437-57del	NP_000093.1:n.437-58_437-57del
NM_000102.4:c.437-58_437-57del MANE Select	NP_000093.1:n.437-58_437-57del