Canonical Allele Identifier: CA1608607566

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583231C= , CM000668.2:g.7583231C=	GRCh38
NC_000006.11:g.7583464C= , CM000668.1:g.7583464C=	GRCh37
NC_000006.10:g.7528463C=	NCBI36
NG_008803.1:g.46595C= , LRG_423:g.46595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4640C=	ENSP00000518230.1:p.Thr1547=
ENST00000379802.8:c.5969C= MANE Select	ENSP00000369129.3:p.Thr1990=
ENST00000379802.7:c.5969C=	ENSP00000369129.3:p.Thr1990=
ENST00000418664.2:c.4172C=	ENSP00000396591.2:p.Thr1391=
NM_001008844.1:c.4172C=	NP_001008844.1:p.Thr1391=
NM_004415.2:c.5969C= , LRG_423t1:c.5969C=	NP_004406.2:p.Thr1990=
XM_011514323.1:c.4640C=	XP_011512625.1:p.Thr1547=
NM_001008844.2:c.4172C=	NP_001008844.1:p.Thr1391=
NM_001319034.1:c.4640C=	NP_001305963.1:p.Thr1547=
NM_004415.3:c.5969C=	NP_004406.2:p.Thr1990=
NM_004415.4:c.5969C= MANE Select	NP_004406.2:p.Thr1990=
NM_001008844.3:c.4172C=	NP_001008844.1:p.Thr1391=
NM_001319034.2:c.4640C=	NP_001305963.1:p.Thr1547=