Canonical Allele Identifier: CA562219401
Gene: SLC25A46 HGNC NCBI

Linked Data

dbSNP Id: rs1174683751

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761188del , CM000667.2:g.110761188del GRCh38
NC_000005.9:g.110096888del , CM000667.1:g.110096888del GRCh37
NC_000005.8:g.110124787del NCBI36
NG_051334.1:g.28053del

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.679-16del MANE Select ENSP00000348211.3:n.679-16del
ENST00000355943.7:c.679-16del ENSP00000348211.3:n.679-16del
ENST00000447245.6:c.679-259del ENSP00000399717.2:n.679-259del
ENST00000502462.6:n.995-16del
ENST00000504098.1:c.241-16del ENSP00000425708.1:n.241-16del
ENST00000509432.1:c.40-16del ENSP00000426604.1:n.40-16del
ENST00000513706.2:n.2279-16del
ENST00000513807.5:c.193-16del ENSP00000421134.1:n.193-16del
NM_001303249.1:c.679-259del NP_001290178.1:n.679-259del
NM_001303250.1:c.406-16del NP_001290179.1:n.406-16del
NM_138773.2:c.679-16del NP_620128.1:n.679-16del
NM_001303249.2:c.679-259del NP_001290178.1:n.679-259del
NM_001303250.2:c.406-16del NP_001290179.1:n.406-16del
NM_138773.3:c.679-16del NP_620128.1:n.679-16del
NR_138151.1:n.953-16del
NM_138773.4:c.679-16del MANE Select NP_620128.1:n.679-16del
NM_001303249.3:c.679-259del NP_001290178.1:n.679-259del
NM_001303250.3:c.406-16del NP_001290179.1:n.406-16del
NR_138151.2:n.918-16del