Canonical Allele Identifier: CA411032921
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750959C>A , CM000684.2:g.27750959C>A GRCh38
NC_000022.10:g.28146947C>A , CM000684.1:g.28146947C>A GRCh37
NC_000022.9:g.26476947C>A NCBI36
NG_023258.1:g.55540G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.444G>T
ENST00000302326.5:c.3919G>T MANE Select ENSP00000304956.4:p.Asp1307Tyr
ENST00000302326.4:c.3919G>T ENSP00000304956.4:p.Asp1307Tyr
ENST00000424656.1:c.272G>T
ENST00000497225.1:n.275G>T
NM_002430.2:c.3919G>T NP_002421.3:p.Asp1307Tyr
NM_002430.3:c.3919G>T MANE Select NP_002421.3:p.Asp1307Tyr