Canonical Allele Identifier: CA1363908897
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345727_50345734delinsCGGGTTAG , CM000665.2:g.50345727_50345734delinsCGGGTTAG GRCh38
NC_000003.11:g.50383158_50383165delinsCGGGTTAG , CM000665.1:g.50383158_50383165delinsCGGGTTAG GRCh37
NC_000003.10:g.50358162_50358169delinsCGGGTTAG NCBI36
NG_023270.1:g.203_210delinsCTAACCCG
NG_042828.1:g.5013_5020delinsCTAACCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-155_-148delinsCTAACCCG ENSP00000231749.3:n.-155_-148delinsCTAACCCG
NM_001308379.1:c.-155_-148delinsCTAACCCG NP_001295308.1:n.-155_-148delinsCTAACCCG
NM_015896.3:c.-155_-148delinsCTAACCCG NP_056980.2:n.-155_-148delinsCTAACCCG
XM_005265216.2:c.-283_-276delinsCTAACCCG XP_005265273.1:n.-283_-276delinsCTAACCCG