Canonical Allele Identifier: CA2677235160

Gene: DSP

Linked Data

• gnomAD v4: 6-7583117-AGACCCAGACTGAGTGTGAGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583122_7583142del , CM000668.2:g.7583122_7583142del	GRCh38
NC_000006.11:g.7583355_7583375del , CM000668.1:g.7583355_7583375del	GRCh37
NC_000006.10:g.7528354_7528374del	NCBI36
NG_008803.1:g.46486_46506del , LRG_423:g.46486_46506del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4531_4551del	ENSP00000518230.1:p.Gln1511_Thr1517del
ENST00000379802.8:c.5860_5880del MANE Select	ENSP00000369129.3:p.Gln1954_Thr1960del
ENST00000379802.7:c.5860_5880del	ENSP00000369129.3:p.Gln1954_Thr1960del
ENST00000418664.2:c.4063_4083del	ENSP00000396591.2:p.Gln1355_Thr1361del
NM_001008844.1:c.4063_4083del	NP_001008844.1:p.Gln1355_Thr1361del
NM_004415.2:c.5860_5880del , LRG_423t1:c.5860_5880del	NP_004406.2:p.Gln1954_Thr1960del
XM_011514323.1:c.4531_4551del	XP_011512625.1:p.Gln1511_Thr1517del
NM_001008844.2:c.4063_4083del	NP_001008844.1:p.Gln1355_Thr1361del
NM_001319034.1:c.4531_4551del	NP_001305963.1:p.Gln1511_Thr1517del
NM_004415.3:c.5860_5880del	NP_004406.2:p.Gln1954_Thr1960del
NM_004415.4:c.5860_5880del MANE Select	NP_004406.2:p.Gln1954_Thr1960del
NM_001008844.3:c.4063_4083del	NP_001008844.1:p.Gln1355_Thr1361del
NM_001319034.2:c.4531_4551del	NP_001305963.1:p.Gln1511_Thr1517del