Canonical Allele Identifier: CA2677223227

Gene: DSP

Linked Data

• gnomAD v4: 6-7568686-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568690_7568692del , CM000668.2:g.7568690_7568692del	GRCh38
NC_000006.11:g.7568923_7568925del , CM000668.1:g.7568923_7568925del	GRCh37
NC_000006.10:g.7513922_7513924del	NCBI36
NG_008803.1:g.32054_32056del , LRG_423:g.32054_32056del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1419+101_1419+103del	ENSP00000518230.1:n.1419+101_1419+103del
ENST00000379802.8:c.1419+101_1419+103del MANE Select	ENSP00000369129.3:n.1419+101_1419+103del
ENST00000379802.7:c.1419+101_1419+103del	ENSP00000369129.3:n.1419+101_1419+103del
ENST00000418664.2:c.1419+101_1419+103del	ENSP00000396591.2:n.1419+101_1419+103del
NM_001008844.1:c.1419+101_1419+103del	NP_001008844.1:n.1419+101_1419+103del
NM_004415.2:c.1419+101_1419+103del , LRG_423t1:c.1419+101_1419+103del	NP_004406.2:n.1419+101_1419+103del
XM_011514323.1:c.1419+101_1419+103del	XP_011512625.1:n.1419+101_1419+103del
NM_001008844.2:c.1419+101_1419+103del	NP_001008844.1:n.1419+101_1419+103del
NM_001319034.1:c.1419+101_1419+103del	NP_001305963.1:n.1419+101_1419+103del
NM_004415.3:c.1419+101_1419+103del	NP_004406.2:n.1419+101_1419+103del
NM_004415.4:c.1419+101_1419+103del MANE Select	NP_004406.2:n.1419+101_1419+103del
NM_001008844.3:c.1419+101_1419+103del	NP_001008844.1:n.1419+101_1419+103del
NM_001319034.2:c.1419+101_1419+103del	NP_001305963.1:n.1419+101_1419+103del