Canonical Allele Identifier: CA1608617823

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565710_7565711delinsCT , CM000668.2:g.7565710_7565711delinsCT	GRCh38
NC_000006.11:g.7565943_7565944delinsCT , CM000668.1:g.7565943_7565944delinsCT	GRCh37
NC_000006.10:g.7510942_7510943delinsCT	NCBI36
NG_008803.1:g.29074_29075delinsCT , LRG_423:g.29074_29075delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+190_939+191delinsCT	ENSP00000518230.1:n.939+190_939+191delinsCT
ENST00000682228.1:n.263+190_263+191delinsCT
ENST00000379802.8:c.939+190_939+191delinsCT MANE Select	ENSP00000369129.3:n.939+190_939+191delinsCT
ENST00000379802.7:c.939+190_939+191delinsCT	ENSP00000369129.3:n.939+190_939+191delinsCT
ENST00000418664.2:c.939+190_939+191delinsCT	ENSP00000396591.2:n.939+190_939+191delinsCT
ENST00000506617.1:n.647_648delinsCT
NM_001008844.1:c.939+190_939+191delinsCT	NP_001008844.1:n.939+190_939+191delinsCT
NM_004415.2:c.939+190_939+191delinsCT , LRG_423t1:c.939+190_939+191delinsCT	NP_004406.2:n.939+190_939+191delinsCT
XM_011514323.1:c.939+190_939+191delinsCT	XP_011512625.1:n.939+190_939+191delinsCT
NM_001008844.2:c.939+190_939+191delinsCT	NP_001008844.1:n.939+190_939+191delinsCT
NM_001319034.1:c.939+190_939+191delinsCT	NP_001305963.1:n.939+190_939+191delinsCT
NM_004415.3:c.939+190_939+191delinsCT	NP_004406.2:n.939+190_939+191delinsCT
NM_004415.4:c.939+190_939+191delinsCT MANE Select	NP_004406.2:n.939+190_939+191delinsCT
NM_001008844.3:c.939+190_939+191delinsCT	NP_001008844.1:n.939+190_939+191delinsCT
NM_001319034.2:c.939+190_939+191delinsCT	NP_001305963.1:n.939+190_939+191delinsCT