Canonical Allele Identifier: CA2399818098

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750924G= , CM000684.2:g.27750924G=	GRCh38
NC_000022.10:g.28146912G= , CM000684.1:g.28146912G=	GRCh37
NC_000022.9:g.26476912G=	NCBI36
NG_023258.1:g.55575C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.479C=
ENST00000302326.5:c.3954C= MANE Select	ENSP00000304956.4:p.Ala1318=
ENST00000302326.4:c.3954C=	ENSP00000304956.4:p.Ala1318=
ENST00000424656.1:c.307C=
ENST00000497225.1:n.310C=
NM_002430.2:c.3954C=	NP_002421.3:p.Ala1318=
NM_002430.3:c.3954C= MANE Select	NP_002421.3:p.Ala1318=