Canonical Allele Identifier: CA2832487455

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2000074del , CM000673.2:g.2000074del GRCh38
NC_000011.9:g.2021304del , CM000673.1:g.2021304del GRCh37
NC_000011.8:g.1977880del NCBI36
NG_016165.1:g.2762del

Transcript Alleles

HGVS Amino-acid Change
NR_131224.1:n.249+1144del (H19)
XM_011520273.1:c.498-11467del (MRPL23) XP_011518575.1:n.498-11467del
XM_011520274.1:c.492-11467del (MRPL23) XP_011518576.1:n.492-11467del
XM_011520275.1:c.498-11467del (MRPL23) XP_011518577.1:n.498-11467del
XM_011520275.2:c.498-11467del (MRPL23) XP_011518577.1:n.498-11467del
NM_001400176.1:c.498-11467del (MRPL23) NP_001387105.1:n.498-11467del