Canonical Allele Identifier: CA1726201263

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93103982C= , CM000669.2:g.93103982C=	GRCh38
NC_000007.13:g.92733295C= , CM000669.1:g.92733295C=	GRCh37
NC_000007.12:g.92571231C=	NCBI36
NG_023419.1:g.19042G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2116G= MANE Select	ENSP00000369292.2:p.Val706=
ENST00000379958.2:c.2116G=	ENSP00000369292.2:p.Val706=
ENST00000446617.1:c.2116G=	ENSP00000414529.1:p.Val706=
ENST00000620985.4:c.2116G=	ENSP00000484636.1:p.Val706=
NM_001193307.1:c.2116G=	NP_001180236.1:p.Val706=
NM_017654.3:c.2116G=	NP_060124.2:p.Val706=
NM_017654.4:c.2116G= MANE Select	NP_060124.2:p.Val706=
NM_001193307.2:c.2116G=	NP_001180236.1:p.Val706=