Canonical Allele Identifier: CA657830394

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949758_43949759insG , CM000685.2:g.43949758_43949759insG GRCh38
NC_000023.10:g.43809004_43809005insG , CM000685.1:g.43809004_43809005insG GRCh37
NC_000023.9:g.43693948_43693949insG NCBI36
NG_009832.1:g.28917_28918insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*40_*41insC (NDP) MANE Select ENSP00000495972.1:n.*40_*41insC
ENST00000647044.1:c.*40_*41insC (NDP) ENSP00000495811.1:n.*40_*41insC
ENST00000378062.5:c.*40_*41insC (NDP) ENSP00000367301.5:n.*40_*41insC
ENST00000470584.1:n.486_487insC (NDP)
NM_000266.3:c.*40_*41insC (NDP) NP_000257.1:n.*40_*41insC
NR_046631.1:n.27_28insG (NDP-AS1)
NM_000266.4:c.*40_*41insC (NDP) MANE Select NP_000257.1:n.*40_*41insC