Canonical Allele Identifier: CA1726201392

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104035_93104037delinsTTG , CM000669.2:g.93104035_93104037delinsTTG	GRCh38
NC_000007.13:g.92733348_92733350delinsTTG , CM000669.1:g.92733348_92733350delinsTTG	GRCh37
NC_000007.12:g.92571284_92571286delinsTTG	NCBI36
NG_023419.1:g.18987_18989delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2061_2063delinsCAA MANE Select	ENSP00000369292.2:p.Gly687=
ENST00000379958.2:c.2061_2063delinsCAA	ENSP00000369292.2:p.Gly687=
ENST00000446617.1:c.2061_2063delinsCAA	ENSP00000414529.1:p.Gly687=
ENST00000620985.4:c.2061_2063delinsCAA	ENSP00000484636.1:p.Gly687=
NM_001193307.1:c.2061_2063delinsCAA	NP_001180236.1:p.Gly687=
NM_017654.3:c.2061_2063delinsCAA	NP_060124.2:p.Gly687=
NM_017654.4:c.2061_2063delinsCAA MANE Select	NP_060124.2:p.Gly687=
NM_001193307.2:c.2061_2063delinsCAA	NP_001180236.1:p.Gly687=