Canonical Allele Identifier: CA1726196720
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101628T= , CM000669.2:g.93101628T= GRCh38
NC_000007.13:g.92730941T= , CM000669.1:g.92730941T= GRCh37
NC_000007.12:g.92568877T= NCBI36
NG_023419.1:g.21396A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4470A= MANE Select ENSP00000369292.2:p.Glu1490=
ENST00000379958.2:c.4470A= ENSP00000369292.2:p.Glu1490=
ENST00000620985.4:c.4470A= ENSP00000484636.1:p.Glu1490=
NM_001193307.1:c.4470A= NP_001180236.1:p.Glu1490=
NM_017654.3:c.4470A= NP_060124.2:p.Glu1490=
NM_017654.4:c.4470A= MANE Select NP_060124.2:p.Glu1490=
NM_001193307.2:c.4470A= NP_001180236.1:p.Glu1490=