Canonical Allele Identifier: CA1608643738

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7554330_7554332delinsCTT , CM000668.2:g.7554330_7554332delinsCTT	GRCh38
NC_000006.11:g.7554563_7554565delinsCTT , CM000668.1:g.7554563_7554565delinsCTT	GRCh37
NC_000006.10:g.7499562_7499564delinsCTT	NCBI36
NG_008803.1:g.17694_17696delinsCTT , LRG_423:g.17694_17696delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683682.2:c.171-1388_171-1386delinsCTT	ENSP00000508162.2:n.171-1388_171-1386delinsCTT
ENST00000710359.1:c.171-1388_171-1386delinsCTT	ENSP00000518230.1:n.171-1388_171-1386delinsCTT
ENST00000683563.1:n.63-1388_63-1386delinsCTT
ENST00000683682.1:c.66-1388_66-1386delinsCTT	ENSP00000508162.1:n.66-1388_66-1386delinsCTT
ENST00000379802.8:c.171-1388_171-1386delinsCTT MANE Select	ENSP00000369129.3:n.171-1388_171-1386delinsCTT
ENST00000379802.7:c.171-1388_171-1386delinsCTT	ENSP00000369129.3:n.171-1388_171-1386delinsCTT
ENST00000418664.2:c.171-1388_171-1386delinsCTT	ENSP00000396591.2:n.171-1388_171-1386delinsCTT
NM_001008844.1:c.171-1388_171-1386delinsCTT	NP_001008844.1:n.171-1388_171-1386delinsCTT
NM_004415.2:c.171-1388_171-1386delinsCTT , LRG_423t1:c.171-1388_171-1386delinsCTT	NP_004406.2:n.171-1388_171-1386delinsCTT
XM_011514323.1:c.171-1388_171-1386delinsCTT	XP_011512625.1:n.171-1388_171-1386delinsCTT
NM_001008844.2:c.171-1388_171-1386delinsCTT	NP_001008844.1:n.171-1388_171-1386delinsCTT
NM_001319034.1:c.171-1388_171-1386delinsCTT	NP_001305963.1:n.171-1388_171-1386delinsCTT
NM_004415.3:c.171-1388_171-1386delinsCTT	NP_004406.2:n.171-1388_171-1386delinsCTT
NM_004415.4:c.171-1388_171-1386delinsCTT MANE Select	NP_004406.2:n.171-1388_171-1386delinsCTT
NM_001008844.3:c.171-1388_171-1386delinsCTT	NP_001008844.1:n.171-1388_171-1386delinsCTT
NM_001319034.2:c.171-1388_171-1386delinsCTT	NP_001305963.1:n.171-1388_171-1386delinsCTT