Canonical Allele Identifier: CA2399817834

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750403T= , CM000684.2:g.27750403T=	GRCh38
NC_000022.10:g.28146391T= , CM000684.1:g.28146391T=	GRCh37
NC_000022.9:g.26476391T=	NCBI36
NG_023258.1:g.56096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.1000A=
ENST00000302326.5:c.*512A= MANE Select	ENSP00000304956.4:n.*512A=
ENST00000302326.4:c.*512A=	ENSP00000304956.4:n.*512A=
ENST00000424656.1:c.456-175A=
NM_002430.2:c.*512A=	NP_002421.3:n.*512A=
NM_002430.3:c.*512A= MANE Select	NP_002421.3:n.*512A=