Canonical Allele Identifier: CA828092666

Gene: DSP

Linked Data

• dbSNP Id: rs1554105404
• gnomAD v3: 6-7554125-A-ACCCC
• gnomAD v4: 6-7554125-A-ACCCC
• MyVariant Identifiers: chr6:g.7554358_7554359insCCCC (hg19) ; chr6:g.7554125_7554126insCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7554128_7554129insCCCC , CM000668.2:g.7554128_7554129insCCCC	GRCh38
NC_000006.11:g.7554361_7554362insCCCC , CM000668.1:g.7554361_7554362insCCCC	GRCh37
NC_000006.10:g.7499360_7499361insCCCC	NCBI36
NG_008803.1:g.17492_17493insCCCC , LRG_423:g.17492_17493insCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683682.2:c.171-1590_171-1589insCCCC	ENSP00000508162.2:n.171-1590_171-1589insCCCC
ENST00000710359.1:c.171-1590_171-1589insCCCC	ENSP00000518230.1:n.171-1590_171-1589insCCCC
ENST00000683563.1:n.63-1590_63-1589insCCCC
ENST00000683682.1:c.66-1590_66-1589insCCCC	ENSP00000508162.1:n.66-1590_66-1589insCCCC
ENST00000379802.8:c.171-1590_171-1589insCCCC MANE Select	ENSP00000369129.3:n.171-1590_171-1589insCCCC
ENST00000379802.7:c.171-1590_171-1589insCCCC	ENSP00000369129.3:n.171-1590_171-1589insCCCC
ENST00000418664.2:c.171-1590_171-1589insCCCC	ENSP00000396591.2:n.171-1590_171-1589insCCCC
NM_001008844.1:c.171-1590_171-1589insCCCC	NP_001008844.1:n.171-1590_171-1589insCCCC
NM_004415.2:c.171-1590_171-1589insCCCC , LRG_423t1:c.171-1590_171-1589insCCCC	NP_004406.2:n.171-1590_171-1589insCCCC
XM_011514323.1:c.171-1590_171-1589insCCCC	XP_011512625.1:n.171-1590_171-1589insCCCC
NM_001008844.2:c.171-1590_171-1589insCCCC	NP_001008844.1:n.171-1590_171-1589insCCCC
NM_001319034.1:c.171-1590_171-1589insCCCC	NP_001305963.1:n.171-1590_171-1589insCCCC
NM_004415.3:c.171-1590_171-1589insCCCC	NP_004406.2:n.171-1590_171-1589insCCCC
NM_004415.4:c.171-1590_171-1589insCCCC MANE Select	NP_004406.2:n.171-1590_171-1589insCCCC
NM_001008844.3:c.171-1590_171-1589insCCCC	NP_001008844.1:n.171-1590_171-1589insCCCC
NM_001319034.2:c.171-1590_171-1589insCCCC	NP_001305963.1:n.171-1590_171-1589insCCCC