Canonical Allele Identifier: CA1825514104

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911913_142911915delinsCAG , CM000670.2:g.142911913_142911915delinsCAG GRCh38
NC_000008.10:g.143993329_143993331delinsCAG , CM000670.1:g.143993329_143993331delinsCAG GRCh37
NC_000008.9:g.143990331_143990333delinsCAG NCBI36
NG_008374.1:g.10929_10931delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.*65_*67delinsCTG (CYP11B2) MANE Select ENSP00000325822.2:n.*65_*67delinsCTG
ENST00000522728.5:c.182-2050_182-2048delinsCAG (GML) ENSP00000430799.1:n.182-2050_182-2048deli...
NM_000498.3:c.*65_*67delinsCTG (CYP11B2) MANE Select NP_000489.3:n.*65_*67delinsCTG
XM_011516877.1:c.*65_*67delinsCTG (CYP11B2) XP_011515179.1:n.*65_*67delinsCTG
XM_011516878.1:c.*65_*67delinsCTG (CYP11B2) XP_011515180.1:n.*65_*67delinsCTG
XM_011516879.1:c.*65_*67delinsCTG (CYP11B2) XP_011515181.1:n.*65_*67delinsCTG
XM_011516970.1:c.215-2050_215-2048delinsCAG (GML) XP_011515272.1:n.215-2050_215-2048delinsC...