Canonical Allele Identifier: CA1608643468

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7553825_7553828delinsGTCT , CM000668.2:g.7553825_7553828delinsGTCT	GRCh38
NC_000006.11:g.7554058_7554061delinsGTCT , CM000668.1:g.7554058_7554061delinsGTCT	GRCh37
NC_000006.10:g.7499057_7499060delinsGTCT	NCBI36
NG_008803.1:g.17189_17192delinsGTCT , LRG_423:g.17189_17192delinsGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683682.2:c.171-1893_171-1890delinsGTCT	ENSP00000508162.2:n.171-1893_171-1890delinsGTCT
ENST00000710359.1:c.171-1893_171-1890delinsGTCT	ENSP00000518230.1:n.171-1893_171-1890delinsGTCT
ENST00000683563.1:n.63-1893_63-1890delinsGTCT
ENST00000683682.1:c.66-1893_66-1890delinsGTCT	ENSP00000508162.1:n.66-1893_66-1890delinsGTCT
ENST00000379802.8:c.171-1893_171-1890delinsGTCT MANE Select	ENSP00000369129.3:n.171-1893_171-1890delinsGTCT
ENST00000379802.7:c.171-1893_171-1890delinsGTCT	ENSP00000369129.3:n.171-1893_171-1890delinsGTCT
ENST00000418664.2:c.171-1893_171-1890delinsGTCT	ENSP00000396591.2:n.171-1893_171-1890delinsGTCT
NM_001008844.1:c.171-1893_171-1890delinsGTCT	NP_001008844.1:n.171-1893_171-1890delinsGTCT
NM_004415.2:c.171-1893_171-1890delinsGTCT , LRG_423t1:c.171-1893_171-1890delinsGTCT	NP_004406.2:n.171-1893_171-1890delinsGTCT
XM_011514323.1:c.171-1893_171-1890delinsGTCT	XP_011512625.1:n.171-1893_171-1890delinsGTCT
NM_001008844.2:c.171-1893_171-1890delinsGTCT	NP_001008844.1:n.171-1893_171-1890delinsGTCT
NM_001319034.1:c.171-1893_171-1890delinsGTCT	NP_001305963.1:n.171-1893_171-1890delinsGTCT
NM_004415.3:c.171-1893_171-1890delinsGTCT	NP_004406.2:n.171-1893_171-1890delinsGTCT
NM_004415.4:c.171-1893_171-1890delinsGTCT MANE Select	NP_004406.2:n.171-1893_171-1890delinsGTCT
NM_001008844.3:c.171-1893_171-1890delinsGTCT	NP_001008844.1:n.171-1893_171-1890delinsGTCT
NM_001319034.2:c.171-1893_171-1890delinsGTCT	NP_001305963.1:n.171-1893_171-1890delinsGTCT