Canonical Allele Identifier: CA2499218556

Gene: DSP

Linked Data

• ClinVar Variation Id: 1072032
• ClinVar RCV Id: RCV001384650 ; RCV001587391
• dbSNP Id: rs2113691528

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579528del , CM000668.2:g.7579528del	GRCh38
NC_000006.11:g.7579761del , CM000668.1:g.7579761del	GRCh37
NC_000006.10:g.7524760del	NCBI36
NG_008803.1:g.42892del , LRG_423:g.42892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.3338del	ENSP00000518230.1:p.Arg1113HisfsTer2
ENST00000379802.8:c.3338del MANE Select	ENSP00000369129.3:p.Arg1113HisfsTer2
ENST00000379802.7:c.3338del	ENSP00000369129.3:p.Arg1113HisfsTer2
ENST00000418664.2:c.3338del	ENSP00000396591.2:p.Arg1113HisfsTer2
NM_001008844.1:c.3338del	NP_001008844.1:p.Arg1113HisfsTer2
NM_004415.2:c.3338del , LRG_423t1:c.3338del	NP_004406.2:p.Arg1113HisfsTer2
XM_011514323.1:c.3338del	XP_011512625.1:p.Arg1113HisfsTer2
NM_001008844.2:c.3338del	NP_001008844.1:p.Arg1113HisfsTer2
NM_001319034.1:c.3338del	NP_001305963.1:p.Arg1113HisfsTer2
NM_004415.3:c.3338del	NP_004406.2:p.Arg1113HisfsTer2
NM_004415.4:c.3338del MANE Select	NP_004406.2:p.Arg1113HisfsTer2
NM_001008844.3:c.3338del	NP_001008844.1:p.Arg1113HisfsTer2
NM_001319034.2:c.3338del	NP_001305963.1:p.Arg1113HisfsTer2