Canonical Allele Identifier: CA1726201417

Gene: SAMD9

Linked Data

• dbSNP Id: rs1791585486

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104041_93104042insTT , CM000669.2:g.93104041_93104042insTT	GRCh38
NC_000007.13:g.92733354_92733355insTT , CM000669.1:g.92733354_92733355insTT	GRCh37
NC_000007.12:g.92571290_92571291insTT	NCBI36
NG_023419.1:g.18982_18983insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2056_2057insAA MANE Select	ENSP00000369292.2:p.Gly686GlufsTer?
ENST00000379958.2:c.2056_2057insAA	ENSP00000369292.2:p.Gly686GlufsTer?
ENST00000446617.1:c.2056_2057insAA	ENSP00000414529.1:p.Gly686GlufsTer?
ENST00000620985.4:c.2056_2057insAA	ENSP00000484636.1:p.Gly686GlufsTer?
NM_001193307.1:c.2056_2057insAA	NP_001180236.1:p.Gly686GlufsTer?
NM_017654.3:c.2056_2057insAA	NP_060124.2:p.Gly686GlufsTer?
NM_017654.4:c.2056_2057insAA MANE Select	NP_060124.2:p.Gly686GlufsTer?
NM_001193307.2:c.2056_2057insAA	NP_001180236.1:p.Gly686GlufsTer?