Canonical Allele Identifier: CA1085708702

Gene: DSP

Linked Data

• gnomAD v3: 6-7567615-CAA-C
• gnomAD v4: 6-7567615-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7567617_7567618del , CM000668.2:g.7567617_7567618del	GRCh38
NC_000006.11:g.7567850_7567851del , CM000668.1:g.7567850_7567851del	GRCh37
NC_000006.10:g.7512849_7512850del	NCBI36
NG_008803.1:g.30981_30982del , LRG_423:g.30981_30982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1141-164_1141-163del	ENSP00000518230.1:n.1141-164_1141-163del
ENST00000682228.1:n.632_633del
ENST00000379802.8:c.1141-164_1141-163del MANE Select	ENSP00000369129.3:n.1141-164_1141-163del
ENST00000379802.7:c.1141-164_1141-163del	ENSP00000369129.3:n.1141-164_1141-163del
ENST00000418664.2:c.1141-164_1141-163del	ENSP00000396591.2:n.1141-164_1141-163del
NM_001008844.1:c.1141-164_1141-163del	NP_001008844.1:n.1141-164_1141-163del
NM_004415.2:c.1141-164_1141-163del , LRG_423t1:c.1141-164_1141-163del	NP_004406.2:n.1141-164_1141-163del
XM_011514323.1:c.1141-164_1141-163del	XP_011512625.1:n.1141-164_1141-163del
NM_001008844.2:c.1141-164_1141-163del	NP_001008844.1:n.1141-164_1141-163del
NM_001319034.1:c.1141-164_1141-163del	NP_001305963.1:n.1141-164_1141-163del
NM_004415.3:c.1141-164_1141-163del	NP_004406.2:n.1141-164_1141-163del
NM_004415.4:c.1141-164_1141-163del MANE Select	NP_004406.2:n.1141-164_1141-163del
NM_001008844.3:c.1141-164_1141-163del	NP_001008844.1:n.1141-164_1141-163del
NM_001319034.2:c.1141-164_1141-163del	NP_001305963.1:n.1141-164_1141-163del