Canonical Allele Identifier: CA1726201531
Gene: SAMD9 HGNC NCBI

Linked Data

dbSNP Id: rs1791586717

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104093del , CM000669.2:g.93104093del GRCh38
NC_000007.13:g.92733406del , CM000669.1:g.92733406del GRCh37
NC_000007.12:g.92571342del NCBI36
NG_023419.1:g.18935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2009del MANE Select ENSP00000369292.2:p.Asn670IlefsTer?
ENST00000379958.2:c.2009del ENSP00000369292.2:p.Asn670IlefsTer?
ENST00000446617.1:c.2009del ENSP00000414529.1:p.Asn670IlefsTer?
ENST00000620985.4:c.2009del ENSP00000484636.1:p.Asn670IlefsTer?
NM_001193307.1:c.2009del NP_001180236.1:p.Asn670IlefsTer?
NM_017654.3:c.2009del NP_060124.2:p.Asn670IlefsTer?
NM_017654.4:c.2009del MANE Select NP_060124.2:p.Asn670IlefsTer?
NM_001193307.2:c.2009del NP_001180236.1:p.Asn670IlefsTer?