Canonical Allele Identifier: CA1608615758

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585763G= , CM000668.2:g.7585763G=	GRCh38
NC_000006.11:g.7585996G= , CM000668.1:g.7585996G=	GRCh37
NC_000006.10:g.7530995G=	NCBI36
NG_008803.1:g.49127G= , LRG_423:g.49127G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7172G=	ENSP00000518230.1:p.Arg2391=
ENST00000379802.8:c.8501G= MANE Select	ENSP00000369129.3:p.Arg2834=
ENST00000379802.7:c.8501G=	ENSP00000369129.3:p.Arg2834=
ENST00000418664.2:c.6704G=	ENSP00000396591.2:p.Arg2235=
NM_001008844.1:c.6704G=	NP_001008844.1:p.Arg2235=
NM_004415.2:c.8501G= , LRG_423t1:c.8501G=	NP_004406.2:p.Arg2834=
XM_011514323.1:c.7172G=	XP_011512625.1:p.Arg2391=
NM_001008844.2:c.6704G=	NP_001008844.1:p.Arg2235=
NM_001319034.1:c.7172G=	NP_001305963.1:p.Arg2391=
NM_004415.3:c.8501G=	NP_004406.2:p.Arg2834=
NM_004415.4:c.8501G= MANE Select	NP_004406.2:p.Arg2834=
NM_001008844.3:c.6704G=	NP_001008844.1:p.Arg2235=
NM_001319034.2:c.7172G=	NP_001305963.1:p.Arg2391=