Canonical Allele Identifier: CA1608623729

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568853_7568855delinsCTG , CM000668.2:g.7568853_7568855delinsCTG	GRCh38
NC_000006.11:g.7569086_7569088delinsCTG , CM000668.1:g.7569086_7569088delinsCTG	GRCh37
NC_000006.10:g.7514085_7514087delinsCTG	NCBI36
NG_008803.1:g.32217_32219delinsCTG , LRG_423:g.32217_32219delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1419+264_1419+266delinsCTG	ENSP00000518230.1:n.1419+264_1419+266delinsCTG
ENST00000379802.8:c.1419+264_1419+266delinsCTG MANE Select	ENSP00000369129.3:n.1419+264_1419+266delinsCTG
ENST00000379802.7:c.1419+264_1419+266delinsCTG	ENSP00000369129.3:n.1419+264_1419+266delinsCTG
ENST00000418664.2:c.1419+264_1419+266delinsCTG	ENSP00000396591.2:n.1419+264_1419+266delinsCTG
NM_001008844.1:c.1419+264_1419+266delinsCTG	NP_001008844.1:n.1419+264_1419+266delinsCTG
NM_004415.2:c.1419+264_1419+266delinsCTG , LRG_423t1:c.1419+264_1419+266delinsCTG	NP_004406.2:n.1419+264_1419+266delinsCTG
XM_011514323.1:c.1419+264_1419+266delinsCTG	XP_011512625.1:n.1419+264_1419+266delinsCTG
NM_001008844.2:c.1419+264_1419+266delinsCTG	NP_001008844.1:n.1419+264_1419+266delinsCTG
NM_001319034.1:c.1419+264_1419+266delinsCTG	NP_001305963.1:n.1419+264_1419+266delinsCTG
NM_004415.3:c.1419+264_1419+266delinsCTG	NP_004406.2:n.1419+264_1419+266delinsCTG
NM_004415.4:c.1419+264_1419+266delinsCTG MANE Select	NP_004406.2:n.1419+264_1419+266delinsCTG
NM_001008844.3:c.1419+264_1419+266delinsCTG	NP_001008844.1:n.1419+264_1419+266delinsCTG
NM_001319034.2:c.1419+264_1419+266delinsCTG	NP_001305963.1:n.1419+264_1419+266delinsCTG