Canonical Allele Identifier: CA1608618669

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7566321T= , CM000668.2:g.7566321T=	GRCh38
NC_000006.11:g.7566554T= , CM000668.1:g.7566554T=	GRCh37
NC_000006.10:g.7511553T=	NCBI36
NG_008803.1:g.29685T= , LRG_423:g.29685T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.940-56T=	ENSP00000518230.1:n.940-56T=
ENST00000682228.1:n.264-56T=
ENST00000379802.8:c.940-56T= MANE Select	ENSP00000369129.3:n.940-56T=
ENST00000379802.7:c.940-56T=	ENSP00000369129.3:n.940-56T=
ENST00000418664.2:c.940-56T=	ENSP00000396591.2:n.940-56T=
NM_001008844.1:c.940-56T=	NP_001008844.1:n.940-56T=
NM_004415.2:c.940-56T= , LRG_423t1:c.940-56T=	NP_004406.2:n.940-56T=
XM_011514323.1:c.940-56T=	XP_011512625.1:n.940-56T=
NM_001008844.2:c.940-56T=	NP_001008844.1:n.940-56T=
NM_001319034.1:c.940-56T=	NP_001305963.1:n.940-56T=
NM_004415.3:c.940-56T=	NP_004406.2:n.940-56T=
NM_004415.4:c.940-56T= MANE Select	NP_004406.2:n.940-56T=
NM_001008844.3:c.940-56T=	NP_001008844.1:n.940-56T=
NM_001319034.2:c.940-56T=	NP_001305963.1:n.940-56T=