Canonical Allele Identifier: CA2187637776
Gene: CYP11A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74339508C= , CM000677.2:g.74339508C= GRCh38
NC_000015.9:g.74631849C= , CM000677.1:g.74631849C= GRCh37
NC_000015.8:g.72418902C= NCBI36
NG_007973.1:g.33234G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268053.11:c.1157+79G= MANE Select ENSP00000268053.6:n.1157+79G=
ENST00000268053.10:c.1157+79G= ENSP00000268053.6:n.1157+79G=
ENST00000358632.8:c.683+79G= ENSP00000351455.4:n.683+79G=
ENST00000435365.5:c.1157+79G= ENSP00000391081.1:n.1157+79G=
NM_000781.2:c.1157+79G= NP_000772.2:n.1157+79G=
NM_001099773.1:c.683+79G= NP_001093243.1:n.683+79G=
NM_000781.3:c.1157+79G= MANE Select NP_000772.2:n.1157+79G=
NM_001099773.2:c.683+79G= NP_001093243.1:n.683+79G=
Search 100 bp 5'
Search 100 bp 3'