Canonical Allele Identifier: CA2677235170

Gene: DSP

Linked Data

• gnomAD v4: 6-7583177-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583182_7583184del , CM000668.2:g.7583182_7583184del	GRCh38
NC_000006.11:g.7583415_7583417del , CM000668.1:g.7583415_7583417del	GRCh37
NC_000006.10:g.7528414_7528416del	NCBI36
NG_008803.1:g.46546_46548del , LRG_423:g.46546_46548del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4591_4593del	ENSP00000518230.1:p.Lys1531del
ENST00000379802.8:c.5920_5922del MANE Select	ENSP00000369129.3:p.Lys1974del
ENST00000379802.7:c.5920_5922del	ENSP00000369129.3:p.Lys1974del
ENST00000418664.2:c.4123_4125del	ENSP00000396591.2:p.Lys1375del
NM_001008844.1:c.4123_4125del	NP_001008844.1:p.Lys1375del
NM_004415.2:c.5920_5922del , LRG_423t1:c.5920_5922del	NP_004406.2:p.Lys1974del
XM_011514323.1:c.4591_4593del	XP_011512625.1:p.Lys1531del
NM_001008844.2:c.4123_4125del	NP_001008844.1:p.Lys1375del
NM_001319034.1:c.4591_4593del	NP_001305963.1:p.Lys1531del
NM_004415.3:c.5920_5922del	NP_004406.2:p.Lys1974del
NM_004415.4:c.5920_5922del MANE Select	NP_004406.2:p.Lys1974del
NM_001008844.3:c.4123_4125del	NP_001008844.1:p.Lys1375del
NM_001319034.2:c.4591_4593del	NP_001305963.1:p.Lys1531del