Canonical Allele Identifier: CA2320171483
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs2057662270

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903823_5903826del , CM000681.2:g.5903823_5903826del GRCh38
NC_000019.9:g.5903834_5903837del , CM000681.1:g.5903834_5903837del GRCh37
NC_000019.8:g.5854834_5854837del NCBI36
NG_027808.1:g.5190_5193del

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.183_186del
NM_001193375.1:c.-116_-113del NP_001180304.1:n.-116_-113del
NM_175614.4:c.-116_-113del NP_783313.1:n.-116_-113del
NR_034166.2:n.190_193del