Canonical Allele Identifier: CA2187637850
Gene: CYP11A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74339566C= , CM000677.2:g.74339566C= GRCh38
NC_000015.9:g.74631907C= , CM000677.1:g.74631907C= GRCh37
NC_000015.8:g.72418960C= NCBI36
NG_007973.1:g.33176G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268053.11:c.1157+21G= MANE Select ENSP00000268053.6:n.1157+21G=
ENST00000268053.10:c.1157+21G= ENSP00000268053.6:n.1157+21G=
ENST00000358632.8:c.683+21G= ENSP00000351455.4:n.683+21G=
ENST00000435365.5:c.1157+21G= ENSP00000391081.1:n.1157+21G=
NM_000781.2:c.1157+21G= NP_000772.2:n.1157+21G=
NM_001099773.1:c.683+21G= NP_001093243.1:n.683+21G=
NM_000781.3:c.1157+21G= MANE Select NP_000772.2:n.1157+21G=
NM_001099773.2:c.683+21G= NP_001093243.1:n.683+21G=
Search 100 bp 5'
Search 100 bp 3'