Canonical Allele Identifier: CA2683736231
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101536del , CM000669.2:g.93101536del GRCh38
NC_000007.13:g.92730849del , CM000669.1:g.92730849del GRCh37
NC_000007.12:g.92568785del NCBI36
NG_023419.1:g.21492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.4566del MANE Select ENSP00000369292.2:p.Val1523SerfsTer19
ENST00000379958.2:c.4566del ENSP00000369292.2:p.Val1523SerfsTer19
ENST00000620985.4:c.4566del ENSP00000484636.1:p.Val1523SerfsTer19
NM_001193307.1:c.4566del NP_001180236.1:p.Val1523SerfsTer19
NM_017654.3:c.4566del NP_060124.2:p.Val1523SerfsTer19
NM_017654.4:c.4566del MANE Select NP_060124.2:p.Val1523SerfsTer19
NM_001193307.2:c.4566del NP_001180236.1:p.Val1523SerfsTer19