Canonical Allele Identifier: CA1608617067

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565369T= , CM000668.2:g.7565369T=	GRCh38
NC_000006.11:g.7565602T= , CM000668.1:g.7565602T=	GRCh37
NC_000006.10:g.7510601T=	NCBI36
NG_008803.1:g.28733T= , LRG_423:g.28733T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.788T=	ENSP00000518230.1:p.Phe263=
ENST00000682228.1:n.112T=
ENST00000379802.8:c.788T= MANE Select	ENSP00000369129.3:p.Phe263=
ENST00000379802.7:c.788T=	ENSP00000369129.3:p.Phe263=
ENST00000418664.2:c.788T=	ENSP00000396591.2:p.Phe263=
ENST00000506617.1:n.306T=
NM_001008844.1:c.788T=	NP_001008844.1:p.Phe263=
NM_004415.2:c.788T= , LRG_423t1:c.788T=	NP_004406.2:p.Phe263=
XM_011514323.1:c.788T=	XP_011512625.1:p.Phe263=
NM_001008844.2:c.788T=	NP_001008844.1:p.Phe263=
NM_001319034.1:c.788T=	NP_001305963.1:p.Phe263=
NM_004415.3:c.788T=	NP_004406.2:p.Phe263=
NM_004415.4:c.788T= MANE Select	NP_004406.2:p.Phe263=
NM_001008844.3:c.788T=	NP_001008844.1:p.Phe263=
NM_001319034.2:c.788T=	NP_001305963.1:p.Phe263=