Canonical Allele Identifier: CA1608623764
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs1758945276

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7568887_7568891del , CM000668.2:g.7568887_7568891del GRCh38
NC_000006.11:g.7569120_7569124del , CM000668.1:g.7569120_7569124del GRCh37
NC_000006.10:g.7514119_7514123del NCBI36
NG_008803.1:g.32251_32255del , LRG_423:g.32251_32255del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.1420-299_1420-295del ENSP00000518230.1:n.1420-299_1420-295del
ENST00000379802.8:c.1420-299_1420-295del MANE Select ENSP00000369129.3:n.1420-299_1420-295del
ENST00000379802.7:c.1420-299_1420-295del ENSP00000369129.3:n.1420-299_1420-295del
ENST00000418664.2:c.1420-299_1420-295del ENSP00000396591.2:n.1420-299_1420-295del
NM_001008844.1:c.1420-299_1420-295del NP_001008844.1:n.1420-299_1420-295del
NM_004415.2:c.1420-299_1420-295del , LRG_423t1:c.1420-299_1420-295del NP_004406.2:n.1420-299_1420-295del
XM_011514323.1:c.1420-299_1420-295del XP_011512625.1:n.1420-299_1420-295del
NM_001008844.2:c.1420-299_1420-295del NP_001008844.1:n.1420-299_1420-295del
NM_001319034.1:c.1420-299_1420-295del NP_001305963.1:n.1420-299_1420-295del
NM_004415.3:c.1420-299_1420-295del NP_004406.2:n.1420-299_1420-295del
NM_004415.4:c.1420-299_1420-295del MANE Select NP_004406.2:n.1420-299_1420-295del
NM_001008844.3:c.1420-299_1420-295del NP_001008844.1:n.1420-299_1420-295del
NM_001319034.2:c.1420-299_1420-295del NP_001305963.1:n.1420-299_1420-295del