Canonical Allele Identifier: CA1608607886

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583351_7583353delinsCTT , CM000668.2:g.7583351_7583353delinsCTT	GRCh38
NC_000006.11:g.7583584_7583586delinsCTT , CM000668.1:g.7583584_7583586delinsCTT	GRCh37
NC_000006.10:g.7528583_7528585delinsCTT	NCBI36
NG_008803.1:g.46715_46717delinsCTT , LRG_423:g.46715_46717delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.4760_4762delinsCTT	ENSP00000518230.1:p.Ser1587=
ENST00000379802.8:c.6089_6091delinsCTT MANE Select	ENSP00000369129.3:p.Ser2030=
ENST00000379802.7:c.6089_6091delinsCTT	ENSP00000369129.3:p.Ser2030=
ENST00000418664.2:c.4292_4294delinsCTT	ENSP00000396591.2:p.Ser1431=
NM_001008844.1:c.4292_4294delinsCTT	NP_001008844.1:p.Ser1431=
NM_004415.2:c.6089_6091delinsCTT , LRG_423t1:c.6089_6091delinsCTT	NP_004406.2:p.Ser2030=
XM_011514323.1:c.4760_4762delinsCTT	XP_011512625.1:p.Ser1587=
NM_001008844.2:c.4292_4294delinsCTT	NP_001008844.1:p.Ser1431=
NM_001319034.1:c.4760_4762delinsCTT	NP_001305963.1:p.Ser1587=
NM_004415.3:c.6089_6091delinsCTT	NP_004406.2:p.Ser2030=
NM_004415.4:c.6089_6091delinsCTT MANE Select	NP_004406.2:p.Ser2030=
NM_001008844.3:c.4292_4294delinsCTT	NP_001008844.1:p.Ser1431=
NM_001319034.2:c.4760_4762delinsCTT	NP_001305963.1:p.Ser1587=