Canonical Allele Identifier: CA2693514206

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949742del , CM000685.2:g.43949742del GRCh38
NC_000023.10:g.43808988del , CM000685.1:g.43808988del GRCh37
NC_000023.9:g.43693932del NCBI36
NG_009832.1:g.28935del

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*58del (NDP) MANE Select ENSP00000495972.1:n.*58del
ENST00000647044.1:c.*58del (NDP) ENSP00000495811.1:n.*58del
ENST00000378062.5:c.*58del (NDP) ENSP00000367301.5:n.*58del
ENST00000470584.1:n.504del (NDP)
NM_000266.3:c.*58del (NDP) NP_000257.1:n.*58del
NR_046631.1:n.11del (NDP-AS1)
NM_000266.4:c.*58del (NDP) MANE Select NP_000257.1:n.*58del