Canonical Allele Identifier: CA1726201473

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104058C= , CM000669.2:g.93104058C=	GRCh38
NC_000007.13:g.92733371C= , CM000669.1:g.92733371C=	GRCh37
NC_000007.12:g.92571307C=	NCBI36
NG_023419.1:g.18966G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379958.3:c.2040G= MANE Select	ENSP00000369292.2:p.Glu680=
ENST00000379958.2:c.2040G=	ENSP00000369292.2:p.Glu680=
ENST00000446617.1:c.2040G=	ENSP00000414529.1:p.Glu680=
ENST00000620985.4:c.2040G=	ENSP00000484636.1:p.Glu680=
NM_001193307.1:c.2040G=	NP_001180236.1:p.Glu680=
NM_017654.3:c.2040G=	NP_060124.2:p.Glu680=
NM_017654.4:c.2040G= MANE Select	NP_060124.2:p.Glu680=
NM_001193307.2:c.2040G=	NP_001180236.1:p.Glu680=