Canonical Allele Identifier: CA411033624
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751054C>G , CM000684.2:g.27751054C>G GRCh38
NC_000022.10:g.28147042C>G , CM000684.1:g.28147042C>G GRCh37
NC_000022.9:g.26477042C>G NCBI36
NG_023258.1:g.55445G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.349G>C
ENST00000302326.5:c.3824G>C MANE Select ENSP00000304956.4:p.Gly1275Ala
ENST00000302326.4:c.3824G>C ENSP00000304956.4:p.Gly1275Ala
ENST00000424656.1:c.177G>C
ENST00000497225.1:n.180G>C
NM_002430.2:c.3824G>C NP_002421.3:p.Gly1275Ala
NM_002430.3:c.3824G>C MANE Select NP_002421.3:p.Gly1275Ala