Canonical Allele Identifier: CA2399817850

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750444A= , CM000684.2:g.27750444A=	GRCh38
NC_000022.10:g.28146432A= , CM000684.1:g.28146432A=	GRCh37
NC_000022.9:g.26476432A=	NCBI36
NG_023258.1:g.56055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.959T=
ENST00000302326.5:c.*471T= MANE Select	ENSP00000304956.4:n.*471T=
ENST00000302326.4:c.*471T=	ENSP00000304956.4:n.*471T=
ENST00000424656.1:c.456-216T=
NM_002430.2:c.*471T=	NP_002421.3:n.*471T=
NM_002430.3:c.*471T= MANE Select	NP_002421.3:n.*471T=