Canonical Allele Identifier: CA1726201317

Gene: SAMD9

Linked Data

• dbSNP Id: rs1791584410

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104015_93104016insTC , CM000669.2:g.93104015_93104016insTC	GRCh38
NC_000007.13:g.92733328_92733329insTC , CM000669.1:g.92733328_92733329insTC	GRCh37
NC_000007.12:g.92571264_92571265insTC	NCBI36
NG_023419.1:g.19008_19009insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2082_2083insGA MANE Select	ENSP00000369292.2:p.Tyr695AspfsTer24
ENST00000379958.2:c.2082_2083insGA	ENSP00000369292.2:p.Tyr695AspfsTer24
ENST00000446617.1:c.2082_2083insGA	ENSP00000414529.1:p.Tyr695AspfsTer24
ENST00000620985.4:c.2082_2083insGA	ENSP00000484636.1:p.Tyr695AspfsTer24
NM_001193307.1:c.2082_2083insGA	NP_001180236.1:p.Tyr695AspfsTer24
NM_017654.3:c.2082_2083insGA	NP_060124.2:p.Tyr695AspfsTer24
NM_017654.4:c.2082_2083insGA MANE Select	NP_060124.2:p.Tyr695AspfsTer24
NM_001193307.2:c.2082_2083insGA	NP_001180236.1:p.Tyr695AspfsTer24