Canonical Allele Identifier: CA1726201527

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104088_93104089delinsAT , CM000669.2:g.93104088_93104089delinsAT	GRCh38
NC_000007.13:g.92733401_92733402delinsAT , CM000669.1:g.92733401_92733402delinsAT	GRCh37
NC_000007.12:g.92571337_92571338delinsAT	NCBI36
NG_023419.1:g.18935_18936delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2009_2010delinsAT MANE Select	ENSP00000369292.2:p.Asn670=
ENST00000379958.2:c.2009_2010delinsAT	ENSP00000369292.2:p.Asn670=
ENST00000446617.1:c.2009_2010delinsAT	ENSP00000414529.1:p.Asn670=
ENST00000620985.4:c.2009_2010delinsAT	ENSP00000484636.1:p.Asn670=
NM_001193307.1:c.2009_2010delinsAT	NP_001180236.1:p.Asn670=
NM_017654.3:c.2009_2010delinsAT	NP_060124.2:p.Asn670=
NM_017654.4:c.2009_2010delinsAT MANE Select	NP_060124.2:p.Asn670=
NM_001193307.2:c.2009_2010delinsAT	NP_001180236.1:p.Asn670=