Canonical Allele Identifier: CA411033617

Gene: MN1

Linked Data

• MyVariant Identifiers: chr22:g.28147040T>G (hg19) ; chr22:g.27751052T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27751052T>G , CM000684.2:g.27751052T>G	GRCh38
NC_000022.10:g.28147040T>G , CM000684.1:g.28147040T>G	GRCh37
NC_000022.9:g.26477040T>G	NCBI36
NG_023258.1:g.55447A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.351A>C
ENST00000302326.5:c.3826A>C MANE Select	ENSP00000304956.4:p.Ser1276Arg
ENST00000302326.4:c.3826A>C	ENSP00000304956.4:p.Ser1276Arg
ENST00000424656.1:c.179A>C
ENST00000497225.1:n.182A>C
NM_002430.2:c.3826A>C	NP_002421.3:p.Ser1276Arg
NM_002430.3:c.3826A>C MANE Select	NP_002421.3:p.Ser1276Arg