Canonical Allele Identifier: CA2677221341

Gene: DSP

Linked Data

• gnomAD v4: 6-7567326-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567328del , CM000668.2:g.7567328del	GRCh38
NC_000006.11:g.7567561del , CM000668.1:g.7567561del	GRCh37
NC_000006.10:g.7512560del	NCBI36
NG_008803.1:g.30692del , LRG_423:g.30692del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.1045-26del	ENSP00000518230.1:n.1045-26del
ENST00000682228.1:n.369-26del
ENST00000379802.8:c.1045-26del MANE Select	ENSP00000369129.3:n.1045-26del
ENST00000379802.7:c.1045-26del	ENSP00000369129.3:n.1045-26del
ENST00000418664.2:c.1045-26del	ENSP00000396591.2:n.1045-26del
NM_001008844.1:c.1045-26del	NP_001008844.1:n.1045-26del
NM_004415.2:c.1045-26del , LRG_423t1:c.1045-26del	NP_004406.2:n.1045-26del
XM_011514323.1:c.1045-26del	XP_011512625.1:n.1045-26del
NM_001008844.2:c.1045-26del	NP_001008844.1:n.1045-26del
NM_001319034.1:c.1045-26del	NP_001305963.1:n.1045-26del
NM_004415.3:c.1045-26del	NP_004406.2:n.1045-26del
NM_004415.4:c.1045-26del MANE Select	NP_004406.2:n.1045-26del
NM_001008844.3:c.1045-26del	NP_001008844.1:n.1045-26del
NM_001319034.2:c.1045-26del	NP_001305963.1:n.1045-26del