Canonical Allele Identifier: CA1608613634

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585199C= , CM000668.2:g.7585199C=	GRCh38
NC_000006.11:g.7585432C= , CM000668.1:g.7585432C=	GRCh37
NC_000006.10:g.7530431C=	NCBI36
NG_008803.1:g.48563C= , LRG_423:g.48563C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6608C=	ENSP00000518230.1:p.Thr2203=
ENST00000379802.8:c.7937C= MANE Select	ENSP00000369129.3:p.Thr2646=
ENST00000379802.7:c.7937C=	ENSP00000369129.3:p.Thr2646=
ENST00000418664.2:c.6140C=	ENSP00000396591.2:p.Thr2047=
NM_001008844.1:c.6140C=	NP_001008844.1:p.Thr2047=
NM_004415.2:c.7937C= , LRG_423t1:c.7937C=	NP_004406.2:p.Thr2646=
XM_011514323.1:c.6608C=	XP_011512625.1:p.Thr2203=
NM_001008844.2:c.6140C=	NP_001008844.1:p.Thr2047=
NM_001319034.1:c.6608C=	NP_001305963.1:p.Thr2203=
NM_004415.3:c.7937C=	NP_004406.2:p.Thr2646=
NM_004415.4:c.7937C= MANE Select	NP_004406.2:p.Thr2646=
NM_001008844.3:c.6140C=	NP_001008844.1:p.Thr2047=
NM_001319034.2:c.6608C=	NP_001305963.1:p.Thr2203=