Canonical Allele Identifier: CA1608613524

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585174G= , CM000668.2:g.7585174G=	GRCh38
NC_000006.11:g.7585407G= , CM000668.1:g.7585407G=	GRCh37
NC_000006.10:g.7530406G=	NCBI36
NG_008803.1:g.48538G= , LRG_423:g.48538G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6583G=	ENSP00000518230.1:p.Glu2195=
ENST00000379802.8:c.7912G= MANE Select	ENSP00000369129.3:p.Glu2638=
ENST00000379802.7:c.7912G=	ENSP00000369129.3:p.Glu2638=
ENST00000418664.2:c.6115G=	ENSP00000396591.2:p.Glu2039=
NM_001008844.1:c.6115G=	NP_001008844.1:p.Glu2039=
NM_004415.2:c.7912G= , LRG_423t1:c.7912G=	NP_004406.2:p.Glu2638=
XM_011514323.1:c.6583G=	XP_011512625.1:p.Glu2195=
NM_001008844.2:c.6115G=	NP_001008844.1:p.Glu2039=
NM_001319034.1:c.6583G=	NP_001305963.1:p.Glu2195=
NM_004415.3:c.7912G=	NP_004406.2:p.Glu2638=
NM_004415.4:c.7912G= MANE Select	NP_004406.2:p.Glu2638=
NM_001008844.3:c.6115G=	NP_001008844.1:p.Glu2039=
NM_001319034.2:c.6583G=	NP_001305963.1:p.Glu2195=