Canonical Allele Identifier: CA2683736271

Gene: SAMD9

Linked Data

• gnomAD v4: 7-93103843-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93103844del , CM000669.2:g.93103844del	GRCh38
NC_000007.13:g.92733157del , CM000669.1:g.92733157del	GRCh37
NC_000007.12:g.92571093del	NCBI36
NG_023419.1:g.19180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2254del MANE Select	ENSP00000369292.2:p.Trp752GlyfsTer3
ENST00000379958.2:c.2254del	ENSP00000369292.2:p.Trp752GlyfsTer3
ENST00000446617.1:c.2254del	ENSP00000414529.1:p.Trp752GlyfsTer3
ENST00000620985.4:c.2254del	ENSP00000484636.1:p.Trp752GlyfsTer3
NM_001193307.1:c.2254del	NP_001180236.1:p.Trp752GlyfsTer3
NM_017654.3:c.2254del	NP_060124.2:p.Trp752GlyfsTer3
NM_017654.4:c.2254del MANE Select	NP_060124.2:p.Trp752GlyfsTer3
NM_001193307.2:c.2254del	NP_001180236.1:p.Trp752GlyfsTer3