Canonical Allele Identifier: CA1608606954
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583031_7583033delinsGAC , CM000668.2:g.7583031_7583033delinsGAC GRCh38
NC_000006.11:g.7583264_7583266delinsGAC , CM000668.1:g.7583264_7583266delinsGAC GRCh37
NC_000006.10:g.7528263_7528265delinsGAC NCBI36
NG_008803.1:g.46395_46397delinsGAC , LRG_423:g.46395_46397delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4440_4442delinsGAC ENSP00000518230.1:p.Glu1480=
ENST00000379802.8:c.5769_5771delinsGAC MANE Select ENSP00000369129.3:p.Glu1923=
ENST00000379802.7:c.5769_5771delinsGAC ENSP00000369129.3:p.Glu1923=
ENST00000418664.2:c.3972_3974delinsGAC ENSP00000396591.2:p.Glu1324=
NM_001008844.1:c.3972_3974delinsGAC NP_001008844.1:p.Glu1324=
NM_004415.2:c.5769_5771delinsGAC , LRG_423t1:c.5769_5771delinsGAC NP_004406.2:p.Glu1923=
XM_011514323.1:c.4440_4442delinsGAC XP_011512625.1:p.Glu1480=
NM_001008844.2:c.3972_3974delinsGAC NP_001008844.1:p.Glu1324=
NM_001319034.1:c.4440_4442delinsGAC NP_001305963.1:p.Glu1480=
NM_004415.3:c.5769_5771delinsGAC NP_004406.2:p.Glu1923=
NM_004415.4:c.5769_5771delinsGAC MANE Select NP_004406.2:p.Glu1923=
NM_001008844.3:c.3972_3974delinsGAC NP_001008844.1:p.Glu1324=
NM_001319034.2:c.4440_4442delinsGAC NP_001305963.1:p.Glu1480=