Canonical Allele Identifier: CA2399817853

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750453A= , CM000684.2:g.27750453A=	GRCh38
NC_000022.10:g.28146441A= , CM000684.1:g.28146441A=	GRCh37
NC_000022.9:g.26476441A=	NCBI36
NG_023258.1:g.56046T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.950T=
ENST00000302326.5:c.*462T= MANE Select	ENSP00000304956.4:n.*462T=
ENST00000302326.4:c.*462T=	ENSP00000304956.4:n.*462T=
ENST00000424656.1:c.456-225T=
NM_002430.2:c.*462T=	NP_002421.3:n.*462T=
NM_002430.3:c.*462T= MANE Select	NP_002421.3:n.*462T=