Canonical Allele Identifier: CA411032928
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750961G>C , CM000684.2:g.27750961G>C GRCh38
NC_000022.10:g.28146949G>C , CM000684.1:g.28146949G>C GRCh37
NC_000022.9:g.26476949G>C NCBI36
NG_023258.1:g.55538C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.442C>G
ENST00000302326.5:c.3917C>G MANE Select ENSP00000304956.4:p.Ser1306Cys
ENST00000302326.4:c.3917C>G ENSP00000304956.4:p.Ser1306Cys
ENST00000424656.1:c.270C>G
ENST00000497225.1:n.273C>G
NM_002430.2:c.3917C>G NP_002421.3:p.Ser1306Cys
NM_002430.3:c.3917C>G MANE Select NP_002421.3:p.Ser1306Cys