Canonical Allele Identifier: CA2573142868

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912625_142912626delinsTA , CM000670.2:g.142912625_142912626delinsTA GRCh38
NC_000008.10:g.143994041_143994042delinsTA , CM000670.1:g.143994041_143994042delinsTA GRCh37
NC_000008.9:g.143991043_143991044delinsTA NCBI36
NG_008374.1:g.10218_10219delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.1302_1303delinsTA (CYP11B2) MANE Select ENSP00000325822.2:p.Gly435Ser
ENST00000522728.5:c.182-1338_182-1337delinsTA (GML) ENSP00000430799.1:n.182-1338_182-1337delinsTA
NM_000498.3:c.1302_1303delinsTA (CYP11B2) MANE Select NP_000489.3:p.Gly435Ser
XM_011516877.1:c.1449_1450delinsTA (CYP11B2) XP_011515179.1:p.Gly484Ser
XM_011516878.1:c.1380_1381delinsTA (CYP11B2) XP_011515180.1:p.Gly461Ser
XM_011516879.1:c.1371_1372delinsTA (CYP11B2) XP_011515181.1:p.Gly458Ser
XM_011516970.1:c.215-1338_215-1337delinsTA (GML) XP_011515272.1:n.215-1338_215-1337delinsTA