Canonical Allele Identifier: CA1932876468

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835066_102835067delinsCT , CM000672.2:g.102835066_102835067delinsCT	GRCh38
NC_000010.10:g.104594823_104594824delinsCT , CM000672.1:g.104594823_104594824delinsCT	GRCh37
NC_000010.9:g.104584813_104584814delinsCT	NCBI36
NG_007955.1:g.7467_7468delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.437-53_437-52delinsAG MANE Select	ENSP00000358903.3:n.437-53_437-52delinsAG
ENST00000638190.1:c.437-53_437-52delinsAG	ENSP00000492539.1:n.437-53_437-52delinsAG
ENST00000638272.1:c.298-1859_298-1858delinsAG	ENSP00000491508.1:n.298-1859_298-1858delinsAG
ENST00000638971.1:c.437-53_437-52delinsAG	ENSP00000492313.1:n.437-53_437-52delinsAG
ENST00000639393.1:c.437-53_437-52delinsAG	ENSP00000492651.1:n.437-53_437-52delinsAG
ENST00000640633.1:n.199-53_199-52delinsAG
ENST00000369887.3:c.437-53_437-52delinsAG	ENSP00000358903.3:n.437-53_437-52delinsAG
ENST00000489268.1:n.691-53_691-52delinsAG
NM_000102.3:c.437-53_437-52delinsAG	NP_000093.1:n.437-53_437-52delinsAG
NM_000102.4:c.437-53_437-52delinsAG MANE Select	NP_000093.1:n.437-53_437-52delinsAG