Canonical Allele Identifier: CA2547961472
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7579669_7579670insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT , CM000668.2:g.7579669_7579670insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT GRCh38
NC_000006.11:g.7579902_7579903insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT , CM000668.1:g.7579902_7579903insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT GRCh37
NC_000006.10:g.7524901_7524902insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NCBI36
NG_008803.1:g.43033_43034insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT , LRG_423:g.43033_43034insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT ENSP00000518230.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSe...
ENST00000379802.8:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT MANE Select ENSP00000369129.3:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSe...
ENST00000379802.7:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT ENSP00000369129.3:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSe...
ENST00000418664.2:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT ENSP00000396591.2:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSe...
NM_001008844.1:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_001008844.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...
NM_004415.2:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT , LRG_423t1:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_004406.2:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSerTh...
XM_011514323.1:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT XP_011512625.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...
NM_001008844.2:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_001008844.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...
NM_001319034.1:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_001305963.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...
NM_004415.3:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_004406.2:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSerTh...
NM_004415.4:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT MANE Select NP_004406.2:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSerTh...
NM_001008844.3:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_001008844.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...
NM_001319034.2:c.3479_3480insATTCTTCTGTTGGTCAAATCTGTCTTCCACAGATTTTCTTCTTCTCTT NP_001305963.1:p.Ser1160_Glu1161insPhePheCysTrpSerAsnLeuSerSe...