Canonical Allele Identifier: CA161989056
Gene: SAMD9 HGNC NCBI

Linked Data

dbSNP Id: rs35485666

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101430dup , CM000669.2:g.93101430dup GRCh38
NC_000007.13:g.92730743dup , CM000669.1:g.92730743dup GRCh37
NC_000007.12:g.92568679dup NCBI36
NG_023419.1:g.21599dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.4673dup MANE Select ENSP00000369292.2:p.Leu1558PhefsTer5
ENST00000379958.2:c.4673dup ENSP00000369292.2:p.Leu1558PhefsTer5
ENST00000620985.4:c.4673dup ENSP00000484636.1:p.Leu1558PhefsTer5
NM_001193307.1:c.4673dup NP_001180236.1:p.Leu1558PhefsTer5
NM_017654.3:c.4673dup NP_060124.2:p.Leu1558PhefsTer5
NM_017654.4:c.4673dup MANE Select NP_060124.2:p.Leu1558PhefsTer5
NM_001193307.2:c.4673dup NP_001180236.1:p.Leu1558PhefsTer5