Canonical Allele Identifier: CA10165932
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs776427712

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750938T>C , CM000684.2:g.27750938T>C GRCh38
NC_000022.10:g.28146926T>C , CM000684.1:g.28146926T>C GRCh37
NC_000022.9:g.26476926T>C NCBI36
NG_023258.1:g.55561A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.465A>G
ENST00000302326.5:c.3940A>G MANE Select ENSP00000304956.4:p.Thr1314Ala
ENST00000302326.4:c.3940A>G ENSP00000304956.4:p.Thr1314Ala
ENST00000424656.1:c.293A>G
ENST00000497225.1:n.296A>G
NM_002430.2:c.3940A>G NP_002421.3:p.Thr1314Ala
NM_002430.3:c.3940A>G MANE Select NP_002421.3:p.Thr1314Ala