Canonical Allele Identifier: CA2399817857

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750467G= , CM000684.2:g.27750467G=	GRCh38
NC_000022.10:g.28146455G= , CM000684.1:g.28146455G=	GRCh37
NC_000022.9:g.26476455G=	NCBI36
NG_023258.1:g.56032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.936C=
ENST00000302326.5:c.*448C= MANE Select	ENSP00000304956.4:n.*448C=
ENST00000302326.4:c.*448C=	ENSP00000304956.4:n.*448C=
ENST00000424656.1:c.456-239C=
NM_002430.2:c.*448C=	NP_002421.3:n.*448C=
NM_002430.3:c.*448C= MANE Select	NP_002421.3:n.*448C=