Canonical Allele Identifier: CA1726201445
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104046A= , CM000669.2:g.93104046A= GRCh38
NC_000007.13:g.92733359A= , CM000669.1:g.92733359A= GRCh37
NC_000007.12:g.92571295A= NCBI36
NG_023419.1:g.18978T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.2052T= MANE Select ENSP00000369292.2:p.Tyr684=
ENST00000379958.2:c.2052T= ENSP00000369292.2:p.Tyr684=
ENST00000446617.1:c.2052T= ENSP00000414529.1:p.Tyr684=
ENST00000620985.4:c.2052T= ENSP00000484636.1:p.Tyr684=
NM_001193307.1:c.2052T= NP_001180236.1:p.Tyr684=
NM_017654.3:c.2052T= NP_060124.2:p.Tyr684=
NM_017654.4:c.2052T= MANE Select NP_060124.2:p.Tyr684=
NM_001193307.2:c.2052T= NP_001180236.1:p.Tyr684=