Canonical Allele Identifier: CA828074807

Gene: DSP

Linked Data

• dbSNP Id: rs1275107193
• gnomAD v4: 6-7566315-TG-T
• MyVariant Identifiers: chr6:g.7566549del (hg19) ; chr6:g.7566316del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7566320del , CM000668.2:g.7566320del	GRCh38
NC_000006.11:g.7566553del , CM000668.1:g.7566553del	GRCh37
NC_000006.10:g.7511552del	NCBI36
NG_008803.1:g.29684del , LRG_423:g.29684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.940-57del	ENSP00000518230.1:n.940-57del
ENST00000682228.1:n.264-57del
ENST00000379802.8:c.940-57del MANE Select	ENSP00000369129.3:n.940-57del
ENST00000379802.7:c.940-57del	ENSP00000369129.3:n.940-57del
ENST00000418664.2:c.940-57del	ENSP00000396591.2:n.940-57del
NM_001008844.1:c.940-57del	NP_001008844.1:n.940-57del
NM_004415.2:c.940-57del , LRG_423t1:c.940-57del	NP_004406.2:n.940-57del
XM_011514323.1:c.940-57del	XP_011512625.1:n.940-57del
NM_001008844.2:c.940-57del	NP_001008844.1:n.940-57del
NM_001319034.1:c.940-57del	NP_001305963.1:n.940-57del
NM_004415.3:c.940-57del	NP_004406.2:n.940-57del
NM_004415.4:c.940-57del MANE Select	NP_004406.2:n.940-57del
NM_001008844.3:c.940-57del	NP_001008844.1:n.940-57del
NM_001319034.2:c.940-57del	NP_001305963.1:n.940-57del