Canonical Allele Identifier: CA1726196333

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93101427A= , CM000669.2:g.93101427A=	GRCh38
NC_000007.13:g.92730740A= , CM000669.1:g.92730740A=	GRCh37
NC_000007.12:g.92568676A=	NCBI36
NG_023419.1:g.21597T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379958.3:c.4671T= MANE Select	ENSP00000369292.2:p.Phe1557=
ENST00000379958.2:c.4671T=	ENSP00000369292.2:p.Phe1557=
ENST00000620985.4:c.4671T=	ENSP00000484636.1:p.Phe1557=
NM_001193307.1:c.4671T=	NP_001180236.1:p.Phe1557=
NM_017654.3:c.4671T=	NP_060124.2:p.Phe1557=
NM_017654.4:c.4671T= MANE Select	NP_060124.2:p.Phe1557=
NM_001193307.2:c.4671T=	NP_001180236.1:p.Phe1557=