Canonical Allele Identifier: CA1608607153
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583082_7583088delinsTAAACTC , CM000668.2:g.7583082_7583088delinsTAAACTC GRCh38
NC_000006.11:g.7583315_7583321delinsTAAACTC , CM000668.1:g.7583315_7583321delinsTAAACTC GRCh37
NC_000006.10:g.7528314_7528320delinsTAAACTC NCBI36
NG_008803.1:g.46446_46452delinsTAAACTC , LRG_423:g.46446_46452delinsTAAACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4491_4497delinsTAAACTC ENSP00000518230.1:p.Asp1497=
ENST00000379802.8:c.5820_5826delinsTAAACTC MANE Select ENSP00000369129.3:p.Asp1940=
ENST00000379802.7:c.5820_5826delinsTAAACTC ENSP00000369129.3:p.Asp1940=
ENST00000418664.2:c.4023_4029delinsTAAACTC ENSP00000396591.2:p.Asp1341=
NM_001008844.1:c.4023_4029delinsTAAACTC NP_001008844.1:p.Asp1341=
NM_004415.2:c.5820_5826delinsTAAACTC , LRG_423t1:c.5820_5826delinsTAAACTC NP_004406.2:p.Asp1940=
XM_011514323.1:c.4491_4497delinsTAAACTC XP_011512625.1:p.Asp1497=
NM_001008844.2:c.4023_4029delinsTAAACTC NP_001008844.1:p.Asp1341=
NM_001319034.1:c.4491_4497delinsTAAACTC NP_001305963.1:p.Asp1497=
NM_004415.3:c.5820_5826delinsTAAACTC NP_004406.2:p.Asp1940=
NM_004415.4:c.5820_5826delinsTAAACTC MANE Select NP_004406.2:p.Asp1940=
NM_001008844.3:c.4023_4029delinsTAAACTC NP_001008844.1:p.Asp1341=
NM_001319034.2:c.4491_4497delinsTAAACTC NP_001305963.1:p.Asp1497=