Canonical Allele Identifier: CA2399818153

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27751049G= , CM000684.2:g.27751049G=	GRCh38
NC_000022.10:g.28147037G= , CM000684.1:g.28147037G=	GRCh37
NC_000022.9:g.26477037G=	NCBI36
NG_023258.1:g.55450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.354C=
ENST00000302326.5:c.3829C= MANE Select	ENSP00000304956.4:p.His1277=
ENST00000302326.4:c.3829C=	ENSP00000304956.4:p.His1277=
ENST00000424656.1:c.182C=
ENST00000497225.1:n.185C=
NM_002430.2:c.3829C=	NP_002421.3:p.His1277=
NM_002430.3:c.3829C= MANE Select	NP_002421.3:p.His1277=