Canonical Allele Identifier: CA1726196328
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101425A= , CM000669.2:g.93101425A= GRCh38
NC_000007.13:g.92730738A= , CM000669.1:g.92730738A= GRCh37
NC_000007.12:g.92568674A= NCBI36
NG_023419.1:g.21599T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.4673T= MANE Select ENSP00000369292.2:p.Leu1558=
ENST00000379958.2:c.4673T= ENSP00000369292.2:p.Leu1558=
ENST00000620985.4:c.4673T= ENSP00000484636.1:p.Leu1558=
NM_001193307.1:c.4673T= NP_001180236.1:p.Leu1558=
NM_017654.3:c.4673T= NP_060124.2:p.Leu1558=
NM_017654.4:c.4673T= MANE Select NP_060124.2:p.Leu1558=
NM_001193307.2:c.4673T= NP_001180236.1:p.Leu1558=