Canonical Allele Identifier: CA2187637863
Gene: CYP11A1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74339576T= , CM000677.2:g.74339576T= GRCh38
NC_000015.9:g.74631917T= , CM000677.1:g.74631917T= GRCh37
NC_000015.8:g.72418970T= NCBI36
NG_007973.1:g.33166A=

Transcript Alleles

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