Canonical Allele Identifier: CA2677234990

Gene: DSP

Linked Data

• gnomAD v4: 6-7583022-TACCAGGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583025_7583033del , CM000668.2:g.7583025_7583033del	GRCh38
NC_000006.11:g.7583258_7583266del , CM000668.1:g.7583258_7583266del	GRCh37
NC_000006.10:g.7528257_7528265del	NCBI36
NG_008803.1:g.46389_46397del , LRG_423:g.46389_46397del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4434_4442del	ENSP00000518230.1:p.Arg1479_Thr1481del
ENST00000379802.8:c.5763_5771del MANE Select	ENSP00000369129.3:p.Arg1922_Thr1924del
ENST00000379802.7:c.5763_5771del	ENSP00000369129.3:p.Arg1922_Thr1924del
ENST00000418664.2:c.3966_3974del	ENSP00000396591.2:p.Arg1323_Thr1325del
NM_001008844.1:c.3966_3974del	NP_001008844.1:p.Arg1323_Thr1325del
NM_004415.2:c.5763_5771del , LRG_423t1:c.5763_5771del	NP_004406.2:p.Arg1922_Thr1924del
XM_011514323.1:c.4434_4442del	XP_011512625.1:p.Arg1479_Thr1481del
NM_001008844.2:c.3966_3974del	NP_001008844.1:p.Arg1323_Thr1325del
NM_001319034.1:c.4434_4442del	NP_001305963.1:p.Arg1479_Thr1481del
NM_004415.3:c.5763_5771del	NP_004406.2:p.Arg1922_Thr1924del
NM_004415.4:c.5763_5771del MANE Select	NP_004406.2:p.Arg1922_Thr1924del
NM_001008844.3:c.3966_3974del	NP_001008844.1:p.Arg1323_Thr1325del
NM_001319034.2:c.4434_4442del	NP_001305963.1:p.Arg1479_Thr1481del