Canonical Allele Identifier: CA1726201546

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104100C= , CM000669.2:g.93104100C=	GRCh38
NC_000007.13:g.92733413C= , CM000669.1:g.92733413C=	GRCh37
NC_000007.12:g.92571349C=	NCBI36
NG_023419.1:g.18924G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.1998G= MANE Select	ENSP00000369292.2:p.Glu666=
ENST00000379958.2:c.1998G=	ENSP00000369292.2:p.Glu666=
ENST00000446617.1:c.1998G=	ENSP00000414529.1:p.Glu666=
ENST00000620985.4:c.1998G=	ENSP00000484636.1:p.Glu666=
NM_001193307.1:c.1998G=	NP_001180236.1:p.Glu666=
NM_017654.3:c.1998G=	NP_060124.2:p.Glu666=
NM_017654.4:c.1998G= MANE Select	NP_060124.2:p.Glu666=
NM_001193307.2:c.1998G=	NP_001180236.1:p.Glu666=