Canonical Allele Identifier: CA2399818111
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750964T= , CM000684.2:g.27750964T= GRCh38
NC_000022.10:g.28146952T= , CM000684.1:g.28146952T= GRCh37
NC_000022.9:g.26476952T= NCBI36
NG_023258.1:g.55535A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.439A=
ENST00000302326.5:c.3914A= MANE Select ENSP00000304956.4:p.His1305=
ENST00000302326.4:c.3914A= ENSP00000304956.4:p.His1305=
ENST00000424656.1:c.267A=
ENST00000497225.1:n.270A=
NM_002430.2:c.3914A= NP_002421.3:p.His1305=
NM_002430.3:c.3914A= MANE Select NP_002421.3:p.His1305=