Canonical Allele Identifier: CA133956241

Gene: DSP

Linked Data

• dbSNP Id: rs1028351189
• gnomAD v3: 6-7568958-CAAAT-C
• gnomAD v4: 6-7568958-CAAAT-C
• MyVariant Identifiers: chr6:g.7569192_7569195del (hg19) ; chr6:g.7568959_7568962del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568970_7568973del , CM000668.2:g.7568970_7568973del	GRCh38
NC_000006.11:g.7569203_7569206del , CM000668.1:g.7569203_7569206del	GRCh37
NC_000006.10:g.7514202_7514205del	NCBI36
NG_008803.1:g.32334_32337del , LRG_423:g.32334_32337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1420-216_1420-213del	ENSP00000518230.1:n.1420-216_1420-213del
ENST00000379802.8:c.1420-216_1420-213del MANE Select	ENSP00000369129.3:n.1420-216_1420-213del
ENST00000379802.7:c.1420-216_1420-213del	ENSP00000369129.3:n.1420-216_1420-213del
ENST00000418664.2:c.1420-216_1420-213del	ENSP00000396591.2:n.1420-216_1420-213del
NM_001008844.1:c.1420-216_1420-213del	NP_001008844.1:n.1420-216_1420-213del
NM_004415.2:c.1420-216_1420-213del , LRG_423t1:c.1420-216_1420-213del	NP_004406.2:n.1420-216_1420-213del
XM_011514323.1:c.1420-216_1420-213del	XP_011512625.1:n.1420-216_1420-213del
NM_001008844.2:c.1420-216_1420-213del	NP_001008844.1:n.1420-216_1420-213del
NM_001319034.1:c.1420-216_1420-213del	NP_001305963.1:n.1420-216_1420-213del
NM_004415.3:c.1420-216_1420-213del	NP_004406.2:n.1420-216_1420-213del
NM_004415.4:c.1420-216_1420-213del MANE Select	NP_004406.2:n.1420-216_1420-213del
NM_001008844.3:c.1420-216_1420-213del	NP_001008844.1:n.1420-216_1420-213del
NM_001319034.2:c.1420-216_1420-213del	NP_001305963.1:n.1420-216_1420-213del