Canonical Allele Identifier: CA1608616232

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585854T= , CM000668.2:g.7585854T=	GRCh38
NC_000006.11:g.7586087T= , CM000668.1:g.7586087T=	GRCh37
NC_000006.10:g.7531086T=	NCBI36
NG_008803.1:g.49218T= , LRG_423:g.49218T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7263T=	ENSP00000518230.1:p.Phe2421=
ENST00000379802.8:c.8592T= MANE Select	ENSP00000369129.3:p.Phe2864=
ENST00000379802.7:c.8592T=	ENSP00000369129.3:p.Phe2864=
ENST00000418664.2:c.6795T=	ENSP00000396591.2:p.Phe2265=
NM_001008844.1:c.6795T=	NP_001008844.1:p.Phe2265=
NM_004415.2:c.8592T= , LRG_423t1:c.8592T=	NP_004406.2:p.Phe2864=
XM_011514323.1:c.7263T=	XP_011512625.1:p.Phe2421=
NM_001008844.2:c.6795T=	NP_001008844.1:p.Phe2265=
NM_001319034.1:c.7263T=	NP_001305963.1:p.Phe2421=
NM_004415.3:c.8592T=	NP_004406.2:p.Phe2864=
NM_004415.4:c.8592T= MANE Select	NP_004406.2:p.Phe2864=
NM_001008844.3:c.6795T=	NP_001008844.1:p.Phe2265=
NM_001319034.2:c.7263T=	NP_001305963.1:p.Phe2421=