Canonical Allele Identifier: CA2399818056
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750862A= , CM000684.2:g.27750862A= GRCh38
NC_000022.10:g.28146850A= , CM000684.1:g.28146850A= GRCh37
NC_000022.9:g.26476850A= NCBI36
NG_023258.1:g.55637T=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.541T=
ENST00000302326.5:c.*53T= MANE Select ENSP00000304956.4:n.*53T=
ENST00000302326.4:c.*53T= ENSP00000304956.4:n.*53T=
ENST00000424656.1:c.369T=
ENST00000497225.1:n.372T=
NM_002430.2:c.*53T= NP_002421.3:n.*53T=
NM_002430.3:c.*53T= MANE Select NP_002421.3:n.*53T=