Canonical Allele Identifier: CA1825515599

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914524_142914534delinsATCCCAAATTC , CM000670.2:g.142914524_142914534delinsATCCCAAATTC	GRCh38
NC_000008.10:g.143995940_143995950delinsATCCCAAATTC , CM000670.1:g.143995940_143995950delinsATCCCAAATTC	GRCh37
NC_000008.9:g.143992942_143992952delinsATCCCAAATTC	NCBI36
NG_008374.1:g.8310_8320delinsGAATTTGGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.800-116_800-106delinsGAATTTGGGAT (CYP11B2) MANE Select	ENSP00000325822.2:n.800-116_800-106delinsGAATTTGGGAT
ENST00000522728.5:c.264+479_264+489delinsATCCCAAATTC (GML)	ENSP00000430799.1:n.264+479_264+489delinsATCCCAAATTC
NM_000498.3:c.800-116_800-106delinsGAATTTGGGAT (CYP11B2) MANE Select	NP_000489.3:n.800-116_800-106delinsGAATTTGGGAT
XM_011516877.1:c.878-116_878-106delinsGAATTTGGGAT (CYP11B2)	XP_011515179.1:n.878-116_878-106delinsGAATTTGGGAT
XM_011516878.1:c.878-116_878-106delinsGAATTTGGGAT (CYP11B2)	XP_011515180.1:n.878-116_878-106delinsGAATTTGGGAT
XM_011516879.1:c.800-116_800-106delinsGAATTTGGGAT (CYP11B2)	XP_011515181.1:n.800-116_800-106delinsGAATTTGGGAT
XM_011516970.1:c.297+479_297+489delinsATCCCAAATTC (GML)	XP_011515272.1:n.297+479_297+489delinsATCCCAAATTC