Canonical Allele Identifier: CA393146954

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74631935T>A (hg19) ; chr15:g.74339594T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339594T>A , CM000677.2:g.74339594T>A	GRCh38
NC_000015.9:g.74631935T>A , CM000677.1:g.74631935T>A	GRCh37
NC_000015.8:g.72418988T>A	NCBI36
NG_007973.1:g.33148A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1150A>T MANE Select	ENSP00000268053.6:p.Thr384Ser
ENST00000268053.10:c.1150A>T	ENSP00000268053.6:p.Thr384Ser
ENST00000358632.8:c.676A>T	ENSP00000351455.4:p.Thr226Ser
ENST00000435365.5:c.1150A>T	ENSP00000391081.1:p.Thr384Ser
ENST00000566674.5:c.676A>T	ENSP00000456941.1:p.Thr226Ser
NM_000781.2:c.1150A>T	NP_000772.2:p.Thr384Ser
NM_001099773.1:c.676A>T	NP_001093243.1:p.Thr226Ser
NM_000781.3:c.1150A>T MANE Select	NP_000772.2:p.Thr384Ser
NM_001099773.2:c.676A>T	NP_001093243.1:p.Thr226Ser