Canonical Allele Identifier: CA1608615428

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579982T= , CM000668.2:g.7579982T=	GRCh38
NC_000006.11:g.7580215T= , CM000668.1:g.7580215T=	GRCh37
NC_000006.10:g.7525214T=	NCBI36
NG_008803.1:g.43346T= , LRG_423:g.43346T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.3792T=	ENSP00000518230.1:p.Thr1264=
ENST00000379802.8:c.3792T= MANE Select	ENSP00000369129.3:p.Thr1264=
ENST00000379802.7:c.3792T=	ENSP00000369129.3:p.Thr1264=
ENST00000418664.2:c.3582+210T=	ENSP00000396591.2:n.3582+210T=
NM_001008844.1:c.3582+210T=	NP_001008844.1:n.3582+210T=
NM_004415.2:c.3792T= , LRG_423t1:c.3792T=	NP_004406.2:p.Thr1264=
XM_011514323.1:c.3792T=	XP_011512625.1:p.Thr1264=
NM_001008844.2:c.3582+210T=	NP_001008844.1:n.3582+210T=
NM_001319034.1:c.3792T=	NP_001305963.1:p.Thr1264=
NM_004415.3:c.3792T=	NP_004406.2:p.Thr1264=
NM_004415.4:c.3792T= MANE Select	NP_004406.2:p.Thr1264=
NM_001008844.3:c.3582+210T=	NP_001008844.1:n.3582+210T=
NM_001319034.2:c.3792T=	NP_001305963.1:p.Thr1264=