Canonical Allele Identifier: CA1608608572

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583581G= , CM000668.2:g.7583581G=	GRCh38
NC_000006.11:g.7583814G= , CM000668.1:g.7583814G=	GRCh37
NC_000006.10:g.7528813G=	NCBI36
NG_008803.1:g.46945G= , LRG_423:g.46945G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.4990G=	ENSP00000518230.1:p.Val1664=
ENST00000379802.8:c.6319G= MANE Select	ENSP00000369129.3:p.Val2107=
ENST00000379802.7:c.6319G=	ENSP00000369129.3:p.Val2107=
ENST00000418664.2:c.4522G=	ENSP00000396591.2:p.Val1508=
NM_001008844.1:c.4522G=	NP_001008844.1:p.Val1508=
NM_004415.2:c.6319G= , LRG_423t1:c.6319G=	NP_004406.2:p.Val2107=
XM_011514323.1:c.4990G=	XP_011512625.1:p.Val1664=
NM_001008844.2:c.4522G=	NP_001008844.1:p.Val1508=
NM_001319034.1:c.4990G=	NP_001305963.1:p.Val1664=
NM_004415.3:c.6319G=	NP_004406.2:p.Val2107=
NM_004415.4:c.6319G= MANE Select	NP_004406.2:p.Val2107=
NM_001008844.3:c.4522G=	NP_001008844.1:p.Val1508=
NM_001319034.2:c.4990G=	NP_001305963.1:p.Val1664=