Canonical Allele Identifier: CA1726196550
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101522G= , CM000669.2:g.93101522G= GRCh38
NC_000007.13:g.92730835G= , CM000669.1:g.92730835G= GRCh37
NC_000007.12:g.92568771G= NCBI36
NG_023419.1:g.21502C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4576C= MANE Select ENSP00000369292.2:p.Leu1526=
ENST00000379958.2:c.4576C= ENSP00000369292.2:p.Leu1526=
ENST00000620985.4:c.4576C= ENSP00000484636.1:p.Leu1526=
NM_001193307.1:c.4576C= NP_001180236.1:p.Leu1526=
NM_017654.3:c.4576C= NP_060124.2:p.Leu1526=
NM_017654.4:c.4576C= MANE Select NP_060124.2:p.Leu1526=
NM_001193307.2:c.4576C= NP_001180236.1:p.Leu1526=