Canonical Allele Identifier: CA2560615705

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7554302del , CM000668.2:g.7554302del	GRCh38
NC_000006.11:g.7554535del , CM000668.1:g.7554535del	GRCh37
NC_000006.10:g.7499534del	NCBI36
NG_008803.1:g.17666del , LRG_423:g.17666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683682.2:c.171-1416del	ENSP00000508162.2:n.171-1416del
ENST00000710359.1:c.171-1416del	ENSP00000518230.1:n.171-1416del
ENST00000683563.1:n.63-1416del
ENST00000683682.1:c.66-1416del	ENSP00000508162.1:n.66-1416del
ENST00000379802.8:c.171-1416del MANE Select	ENSP00000369129.3:n.171-1416del
ENST00000379802.7:c.171-1416del	ENSP00000369129.3:n.171-1416del
ENST00000418664.2:c.171-1416del	ENSP00000396591.2:n.171-1416del
NM_001008844.1:c.171-1416del	NP_001008844.1:n.171-1416del
NM_004415.2:c.171-1416del , LRG_423t1:c.171-1416del	NP_004406.2:n.171-1416del
XM_011514323.1:c.171-1416del	XP_011512625.1:n.171-1416del
NM_001008844.2:c.171-1416del	NP_001008844.1:n.171-1416del
NM_001319034.1:c.171-1416del	NP_001305963.1:n.171-1416del
NM_004415.3:c.171-1416del	NP_004406.2:n.171-1416del
NM_004415.4:c.171-1416del MANE Select	NP_004406.2:n.171-1416del
NM_001008844.3:c.171-1416del	NP_001008844.1:n.171-1416del
NM_001319034.2:c.171-1416del	NP_001305963.1:n.171-1416del