Canonical Allele Identifier: CA2629468573

Gene: CYP11A1

Linked Data

• gnomAD v4: 15-74339773-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339773A>G , CM000677.2:g.74339773A>G	GRCh38
NC_000015.9:g.74632114A>G , CM000677.1:g.74632114A>G	GRCh37
NC_000015.8:g.72419167A>G	NCBI36
NG_007973.1:g.32969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.991-20T>C MANE Select	ENSP00000268053.6:n.991-20T>C
ENST00000268053.10:c.991-20T>C	ENSP00000268053.6:n.991-20T>C
ENST00000358632.8:c.517-20T>C	ENSP00000351455.4:n.517-20T>C
ENST00000435365.5:c.991-20T>C	ENSP00000391081.1:n.991-20T>C
ENST00000566674.5:c.517-20T>C	ENSP00000456941.1:n.517-20T>C
NM_000781.2:c.991-20T>C	NP_000772.2:n.991-20T>C
NM_001099773.1:c.517-20T>C	NP_001093243.1:n.517-20T>C
NM_000781.3:c.991-20T>C MANE Select	NP_000772.2:n.991-20T>C
NM_001099773.2:c.517-20T>C	NP_001093243.1:n.517-20T>C