Canonical Allele Identifier: CA1608607650

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583260_7583262delinsTCA , CM000668.2:g.7583260_7583262delinsTCA	GRCh38
NC_000006.11:g.7583493_7583495delinsTCA , CM000668.1:g.7583493_7583495delinsTCA	GRCh37
NC_000006.10:g.7528492_7528494delinsTCA	NCBI36
NG_008803.1:g.46624_46626delinsTCA , LRG_423:g.46624_46626delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4669_4671delinsTCA	ENSP00000518230.1:p.Ser1557=
ENST00000379802.8:c.5998_6000delinsTCA MANE Select	ENSP00000369129.3:p.Ser2000=
ENST00000379802.7:c.5998_6000delinsTCA	ENSP00000369129.3:p.Ser2000=
ENST00000418664.2:c.4201_4203delinsTCA	ENSP00000396591.2:p.Ser1401=
NM_001008844.1:c.4201_4203delinsTCA	NP_001008844.1:p.Ser1401=
NM_004415.2:c.5998_6000delinsTCA , LRG_423t1:c.5998_6000delinsTCA	NP_004406.2:p.Ser2000=
XM_011514323.1:c.4669_4671delinsTCA	XP_011512625.1:p.Ser1557=
NM_001008844.2:c.4201_4203delinsTCA	NP_001008844.1:p.Ser1401=
NM_001319034.1:c.4669_4671delinsTCA	NP_001305963.1:p.Ser1557=
NM_004415.3:c.5998_6000delinsTCA	NP_004406.2:p.Ser2000=
NM_004415.4:c.5998_6000delinsTCA MANE Select	NP_004406.2:p.Ser2000=
NM_001008844.3:c.4201_4203delinsTCA	NP_001008844.1:p.Ser1401=
NM_001319034.2:c.4669_4671delinsTCA	NP_001305963.1:p.Ser1557=