Canonical Allele Identifier: CA1120128558

Linked Data

dbSNP Id: rs776404064

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912544_142912549del , CM000670.2:g.142912544_142912549del GRCh38
NC_000008.10:g.143993960_143993965del , CM000670.1:g.143993960_143993965del GRCh37
NC_000008.9:g.143990962_143990967del NCBI36
NG_008374.1:g.10304_10309del

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1388_1393del (CYP11B2) MANE Select ENSP00000325822.2:p.Leu463_Leu464del
ENST00000522728.5:c.182-1419_182-1414del (GML) ENSP00000430799.1:n.182-1419_182-1414del
NM_000498.3:c.1388_1393del (CYP11B2) MANE Select NP_000489.3:p.Leu463_Leu464del
XM_011516877.1:c.1535_1540del (CYP11B2) XP_011515179.1:p.Leu512_Leu513del
XM_011516878.1:c.1466_1471del (CYP11B2) XP_011515180.1:p.Leu489_Leu490del
XM_011516879.1:c.1457_1462del (CYP11B2) XP_011515181.1:p.Leu486_Leu487del
XM_011516970.1:c.215-1419_215-1414del (GML) XP_011515272.1:n.215-1419_215-1414del