Canonical Allele Identifier: CA2399817949
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750650A= , CM000684.2:g.27750650A= GRCh38
NC_000022.10:g.28146638A= , CM000684.1:g.28146638A= GRCh37
NC_000022.9:g.26476638A= NCBI36
NG_023258.1:g.55849T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.753T=
ENST00000302326.5:c.*265T= MANE Select ENSP00000304956.4:n.*265T=
ENST00000302326.4:c.*265T= ENSP00000304956.4:n.*265T=
ENST00000424656.1:c.455+126T=
NM_002430.2:c.*265T= NP_002421.3:n.*265T=
NM_002430.3:c.*265T= MANE Select NP_002421.3:n.*265T=