Canonical Allele Identifier: CA1726201337

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104021_93104025delinsTCCAC , CM000669.2:g.93104021_93104025delinsTCCAC	GRCh38
NC_000007.13:g.92733334_92733338delinsTCCAC , CM000669.1:g.92733334_92733338delinsTCCAC	GRCh37
NC_000007.12:g.92571270_92571274delinsTCCAC	NCBI36
NG_023419.1:g.18999_19003delinsGTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2073_2077delinsGTGGA MANE Select	ENSP00000369292.2:p.Trp691=
ENST00000379958.2:c.2073_2077delinsGTGGA	ENSP00000369292.2:p.Trp691=
ENST00000446617.1:c.2073_2077delinsGTGGA	ENSP00000414529.1:p.Trp691=
ENST00000620985.4:c.2073_2077delinsGTGGA	ENSP00000484636.1:p.Trp691=
NM_001193307.1:c.2073_2077delinsGTGGA	NP_001180236.1:p.Trp691=
NM_017654.3:c.2073_2077delinsGTGGA	NP_060124.2:p.Trp691=
NM_017654.4:c.2073_2077delinsGTGGA MANE Select	NP_060124.2:p.Trp691=
NM_001193307.2:c.2073_2077delinsGTGGA	NP_001180236.1:p.Trp691=