Canonical Allele Identifier: CA920351007
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1568968814

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750856del , CM000684.2:g.27750856del GRCh38
NC_000022.10:g.28146844del , CM000684.1:g.28146844del GRCh37
NC_000022.9:g.26476844del NCBI36
NG_023258.1:g.55647del

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.551del
ENST00000302326.5:c.*63del MANE Select ENSP00000304956.4:n.*63del
ENST00000302326.4:c.*63del ENSP00000304956.4:n.*63del
ENST00000424656.1:c.379del
ENST00000497225.1:n.382del
NM_002430.2:c.*63del NP_002421.3:n.*63del
NM_002430.3:c.*63del MANE Select NP_002421.3:n.*63del