Canonical Allele Identifier: CA2399817829

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750387G= , CM000684.2:g.27750387G=	GRCh38
NC_000022.10:g.28146375G= , CM000684.1:g.28146375G=	GRCh37
NC_000022.9:g.26476375G=	NCBI36
NG_023258.1:g.56112C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.1016C=
ENST00000302326.5:c.*528C= MANE Select	ENSP00000304956.4:n.*528C=
ENST00000302326.4:c.*528C=	ENSP00000304956.4:n.*528C=
ENST00000424656.1:c.456-159C=
NM_002430.2:c.*528C=	NP_002421.3:n.*528C=
NM_002430.3:c.*528C= MANE Select	NP_002421.3:n.*528C=