Canonical Allele Identifier: CA2693514207

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949758dup , CM000685.2:g.43949758dup GRCh38
NC_000023.10:g.43809004dup , CM000685.1:g.43809004dup GRCh37
NC_000023.9:g.43693948dup NCBI36
NG_009832.1:g.28918dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*41dup (NDP) MANE Select ENSP00000495972.1:n.*41dup
ENST00000647044.1:c.*41dup (NDP) ENSP00000495811.1:n.*41dup
ENST00000378062.5:c.*41dup (NDP) ENSP00000367301.5:n.*41dup
ENST00000470584.1:n.487dup (NDP)
NM_000266.3:c.*41dup (NDP) NP_000257.1:n.*41dup
NR_046631.1:n.27dup (NDP-AS1)
NM_000266.4:c.*41dup (NDP) MANE Select NP_000257.1:n.*41dup