Canonical Allele Identifier: CA1726201206

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93103971_93103989delinsATCCCTTTTGACAAAAGGT , CM000669.2:g.93103971_93103989delinsATCCCTTTTGACAAAAGGT	GRCh38
NC_000007.13:g.92733284_92733302delinsATCCCTTTTGACAAAAGGT , CM000669.1:g.92733284_92733302delinsATCCCTTTTGACAAAAGGT	GRCh37
NC_000007.12:g.92571220_92571238delinsATCCCTTTTGACAAAAGGT	NCBI36
NG_023419.1:g.19035_19053delinsACCTTTTGTCAAAAGGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2109_2127delinsACCTTTTGTCAAAAGGGAT MANE Select	ENSP00000369292.2:p.Ser703=
ENST00000379958.2:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	ENSP00000369292.2:p.Ser703=
ENST00000446617.1:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	ENSP00000414529.1:p.Ser703=
ENST00000620985.4:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	ENSP00000484636.1:p.Ser703=
NM_001193307.1:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	NP_001180236.1:p.Ser703=
NM_017654.3:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	NP_060124.2:p.Ser703=
NM_017654.4:c.2109_2127delinsACCTTTTGTCAAAAGGGAT MANE Select	NP_060124.2:p.Ser703=
NM_001193307.2:c.2109_2127delinsACCTTTTGTCAAAAGGGAT	NP_001180236.1:p.Ser703=