Canonical Allele Identifier: CA2399818046
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750849T= , CM000684.2:g.27750849T= GRCh38
NC_000022.10:g.28146837T= , CM000684.1:g.28146837T= GRCh37
NC_000022.9:g.26476837T= NCBI36
NG_023258.1:g.55650A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.554A=
ENST00000302326.5:c.*66A= MANE Select ENSP00000304956.4:n.*66A=
ENST00000302326.4:c.*66A= ENSP00000304956.4:n.*66A=
ENST00000424656.1:c.382A=
ENST00000497225.1:n.385A=
NM_002430.2:c.*66A= NP_002421.3:n.*66A=
NM_002430.3:c.*66A= MANE Select NP_002421.3:n.*66A=