Canonical Allele Identifier: CA2740094257

Gene: DSP

Linked Data

• ClinVar Variation Id: 2941971
• ClinVar RCV Id: RCV003802993

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579719del , CM000668.2:g.7579719del	GRCh38
NC_000006.11:g.7579952del , CM000668.1:g.7579952del	GRCh37
NC_000006.10:g.7524951del	NCBI36
NG_008803.1:g.43083del , LRG_423:g.43083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.3529del	ENSP00000518230.1:p.Leu1177TyrfsTer19
ENST00000379802.8:c.3529del MANE Select	ENSP00000369129.3:p.Leu1177TyrfsTer19
ENST00000379802.7:c.3529del	ENSP00000369129.3:p.Leu1177TyrfsTer19
ENST00000418664.2:c.3529del	ENSP00000396591.2:p.Leu1177TyrfsTer?
NM_001008844.1:c.3529del	NP_001008844.1:p.Leu1177TyrfsTer?
NM_004415.2:c.3529del , LRG_423t1:c.3529del	NP_004406.2:p.Leu1177TyrfsTer19
XM_011514323.1:c.3529del	XP_011512625.1:p.Leu1177TyrfsTer19
NM_001008844.2:c.3529del	NP_001008844.1:p.Leu1177TyrfsTer?
NM_001319034.1:c.3529del	NP_001305963.1:p.Leu1177TyrfsTer19
NM_004415.3:c.3529del	NP_004406.2:p.Leu1177TyrfsTer19
NM_004415.4:c.3529del MANE Select	NP_004406.2:p.Leu1177TyrfsTer19
NM_001008844.3:c.3529del	NP_001008844.1:p.Leu1177TyrfsTer?
NM_001319034.2:c.3529del	NP_001305963.1:p.Leu1177TyrfsTer19