Canonical Allele Identifier: CA1608613838

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579429_7579430delinsAG , CM000668.2:g.7579429_7579430delinsAG	GRCh38
NC_000006.11:g.7579662_7579663delinsAG , CM000668.1:g.7579662_7579663delinsAG	GRCh37
NC_000006.10:g.7524661_7524662delinsAG	NCBI36
NG_008803.1:g.42793_42794delinsAG , LRG_423:g.42793_42794delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.3239_3240delinsAG	ENSP00000518230.1:p.Glu1080=
ENST00000379802.8:c.3239_3240delinsAG MANE Select	ENSP00000369129.3:p.Glu1080=
ENST00000379802.7:c.3239_3240delinsAG	ENSP00000369129.3:p.Glu1080=
ENST00000418664.2:c.3239_3240delinsAG	ENSP00000396591.2:p.Glu1080=
NM_001008844.1:c.3239_3240delinsAG	NP_001008844.1:p.Glu1080=
NM_004415.2:c.3239_3240delinsAG , LRG_423t1:c.3239_3240delinsAG	NP_004406.2:p.Glu1080=
XM_011514323.1:c.3239_3240delinsAG	XP_011512625.1:p.Glu1080=
NM_001008844.2:c.3239_3240delinsAG	NP_001008844.1:p.Glu1080=
NM_001319034.1:c.3239_3240delinsAG	NP_001305963.1:p.Glu1080=
NM_004415.3:c.3239_3240delinsAG	NP_004406.2:p.Glu1080=
NM_004415.4:c.3239_3240delinsAG MANE Select	NP_004406.2:p.Glu1080=
NM_001008844.3:c.3239_3240delinsAG	NP_001008844.1:p.Glu1080=
NM_001319034.2:c.3239_3240delinsAG	NP_001305963.1:p.Glu1080=