Canonical Allele Identifier: CA368177532
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4576C>A MANE Select ENSP00000369292.2:p.Leu1526Ile
ENST00000379958.2:c.4576C>A ENSP00000369292.2:p.Leu1526Ile
ENST00000620985.4:c.4576C>A ENSP00000484636.1:p.Leu1526Ile
NM_001193307.1:c.4576C>A NP_001180236.1:p.Leu1526Ile
NM_017654.3:c.4576C>A NP_060124.2:p.Leu1526Ile
NM_017654.4:c.4576C>A MANE Select NP_060124.2:p.Leu1526Ile
NM_001193307.2:c.4576C>A NP_001180236.1:p.Leu1526Ile