Canonical Allele Identifier: CA1608606684

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7582941C= , CM000668.2:g.7582941C=	GRCh38
NC_000006.11:g.7583174C= , CM000668.1:g.7583174C=	GRCh37
NC_000006.10:g.7528173C=	NCBI36
NG_008803.1:g.46305C= , LRG_423:g.46305C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4350C=	ENSP00000518230.1:p.Asn1450=
ENST00000379802.8:c.5679C= MANE Select	ENSP00000369129.3:p.Asn1893=
ENST00000379802.7:c.5679C=	ENSP00000369129.3:p.Asn1893=
ENST00000418664.2:c.3882C=	ENSP00000396591.2:p.Asn1294=
NM_001008844.1:c.3882C=	NP_001008844.1:p.Asn1294=
NM_004415.2:c.5679C= , LRG_423t1:c.5679C=	NP_004406.2:p.Asn1893=
XM_011514323.1:c.4350C=	XP_011512625.1:p.Asn1450=
NM_001008844.2:c.3882C=	NP_001008844.1:p.Asn1294=
NM_001319034.1:c.4350C=	NP_001305963.1:p.Asn1450=
NM_004415.3:c.5679C=	NP_004406.2:p.Asn1893=
NM_004415.4:c.5679C= MANE Select	NP_004406.2:p.Asn1893=
NM_001008844.3:c.3882C=	NP_001008844.1:p.Asn1294=
NM_001319034.2:c.4350C=	NP_001305963.1:p.Asn1450=