Canonical Allele Identifier: CA1608614417

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585428T= , CM000668.2:g.7585428T=	GRCh38
NC_000006.11:g.7585661T= , CM000668.1:g.7585661T=	GRCh37
NC_000006.10:g.7530660T=	NCBI36
NG_008803.1:g.48792T= , LRG_423:g.48792T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6837T=	ENSP00000518230.1:p.Ala2279=
ENST00000379802.8:c.8166T= MANE Select	ENSP00000369129.3:p.Ala2722=
ENST00000379802.7:c.8166T=	ENSP00000369129.3:p.Ala2722=
ENST00000418664.2:c.6369T=	ENSP00000396591.2:p.Ala2123=
NM_001008844.1:c.6369T=	NP_001008844.1:p.Ala2123=
NM_004415.2:c.8166T= , LRG_423t1:c.8166T=	NP_004406.2:p.Ala2722=
XM_011514323.1:c.6837T=	XP_011512625.1:p.Ala2279=
NM_001008844.2:c.6369T=	NP_001008844.1:p.Ala2123=
NM_001319034.1:c.6837T=	NP_001305963.1:p.Ala2279=
NM_004415.3:c.8166T=	NP_004406.2:p.Ala2722=
NM_004415.4:c.8166T= MANE Select	NP_004406.2:p.Ala2722=
NM_001008844.3:c.6369T=	NP_001008844.1:p.Ala2123=
NM_001319034.2:c.6837T=	NP_001305963.1:p.Ala2279=