Canonical Allele Identifier: CA1726201192
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93103960C= , CM000669.2:g.93103960C= GRCh38
NC_000007.13:g.92733273C= , CM000669.1:g.92733273C= GRCh37
NC_000007.12:g.92571209C= NCBI36
NG_023419.1:g.19064G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2138G= MANE Select ENSP00000369292.2:p.Arg713=
ENST00000379958.2:c.2138G= ENSP00000369292.2:p.Arg713=
ENST00000446617.1:c.2138G= ENSP00000414529.1:p.Arg713=
ENST00000620985.4:c.2138G= ENSP00000484636.1:p.Arg713=
NM_001193307.1:c.2138G= NP_001180236.1:p.Arg713=
NM_017654.3:c.2138G= NP_060124.2:p.Arg713=
NM_017654.4:c.2138G= MANE Select NP_060124.2:p.Arg713=
NM_001193307.2:c.2138G= NP_001180236.1:p.Arg713=