Canonical Allele Identifier: CA448517804

Gene: DSP

Linked Data

• COSMIC: COSM1621922
• MyVariant Identifiers: chr6:g.7565612del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565380del , CM000668.2:g.7565380del	GRCh38
NC_000006.11:g.7565613del , CM000668.1:g.7565613del	GRCh37
NC_000006.10:g.7510612del	NCBI36
NG_008803.1:g.28744del , LRG_423:g.28744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.799del	ENSP00000518230.1:p.Asp267IlefsTer?
ENST00000682228.1:n.123del
ENST00000379802.8:c.799del MANE Select	ENSP00000369129.3:p.Asp267IlefsTer?
ENST00000379802.7:c.799del	ENSP00000369129.3:p.Asp267IlefsTer?
ENST00000418664.2:c.799del	ENSP00000396591.2:p.Asp267IlefsTer?
ENST00000506617.1:n.317del
NM_001008844.1:c.799del	NP_001008844.1:p.Asp267IlefsTer?
NM_004415.2:c.799del , LRG_423t1:c.799del	NP_004406.2:p.Asp267IlefsTer?
XM_011514323.1:c.799del	XP_011512625.1:p.Asp267IlefsTer?
NM_001008844.2:c.799del	NP_001008844.1:p.Asp267IlefsTer?
NM_001319034.1:c.799del	NP_001305963.1:p.Asp267IlefsTer?
NM_004415.3:c.799del	NP_004406.2:p.Asp267IlefsTer?
NM_004415.4:c.799del MANE Select	NP_004406.2:p.Asp267IlefsTer?
NM_001008844.3:c.799del	NP_001008844.1:p.Asp267IlefsTer?
NM_001319034.2:c.799del	NP_001305963.1:p.Asp267IlefsTer?