Canonical Allele Identifier: CA2399818024
Gene: MN1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750802C= , CM000684.2:g.27750802C= GRCh38
NC_000022.10:g.28146790C= , CM000684.1:g.28146790C= GRCh37
NC_000022.9:g.26476790C= NCBI36
NG_023258.1:g.55697G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.601G=
ENST00000302326.5:c.*113G= MANE Select ENSP00000304956.4:n.*113G=
ENST00000302326.4:c.*113G= ENSP00000304956.4:n.*113G=
ENST00000424656.1:c.429G=
ENST00000497225.1:n.432G=
NM_002430.2:c.*113G= NP_002421.3:n.*113G=
NM_002430.3:c.*113G= MANE Select NP_002421.3:n.*113G=
Search 100 bp 5'
Search 100 bp 3'