Canonical Allele Identifier: CA2399818045
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750848T= , CM000684.2:g.27750848T= GRCh38
NC_000022.10:g.28146836T= , CM000684.1:g.28146836T= GRCh37
NC_000022.9:g.26476836T= NCBI36
NG_023258.1:g.55651A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.555A=
ENST00000302326.5:c.*67A= MANE Select ENSP00000304956.4:n.*67A=
ENST00000302326.4:c.*67A= ENSP00000304956.4:n.*67A=
ENST00000424656.1:c.383A=
ENST00000497225.1:n.386A=
NM_002430.2:c.*67A= NP_002421.3:n.*67A=
NM_002430.3:c.*67A= MANE Select NP_002421.3:n.*67A=