Canonical Allele Identifier: CA1726201578
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104116T= , CM000669.2:g.93104116T= GRCh38
NC_000007.13:g.92733429T= , CM000669.1:g.92733429T= GRCh37
NC_000007.12:g.92571365T= NCBI36
NG_023419.1:g.18908A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.1982A= MANE Select ENSP00000369292.2:p.Glu661=
ENST00000379958.2:c.1982A= ENSP00000369292.2:p.Glu661=
ENST00000446617.1:c.1982A= ENSP00000414529.1:p.Glu661=
ENST00000620985.4:c.1982A= ENSP00000484636.1:p.Glu661=
NM_001193307.1:c.1982A= NP_001180236.1:p.Glu661=
NM_017654.3:c.1982A= NP_060124.2:p.Glu661=
NM_017654.4:c.1982A= MANE Select NP_060124.2:p.Glu661=
NM_001193307.2:c.1982A= NP_001180236.1:p.Glu661=