Canonical Allele Identifier: CA1726196577
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101537C= , CM000669.2:g.93101537C= GRCh38
NC_000007.13:g.92730850C= , CM000669.1:g.92730850C= GRCh37
NC_000007.12:g.92568786C= NCBI36
NG_023419.1:g.21487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.4561G= MANE Select ENSP00000369292.2:p.Glu1521=
ENST00000379958.2:c.4561G= ENSP00000369292.2:p.Glu1521=
ENST00000620985.4:c.4561G= ENSP00000484636.1:p.Glu1521=
NM_001193307.1:c.4561G= NP_001180236.1:p.Glu1521=
NM_017654.3:c.4561G= NP_060124.2:p.Glu1521=
NM_017654.4:c.4561G= MANE Select NP_060124.2:p.Glu1521=
NM_001193307.2:c.4561G= NP_001180236.1:p.Glu1521=