Canonical Allele Identifier: CA1608616968

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565317G= , CM000668.2:g.7565317G=	GRCh38
NC_000006.11:g.7565550G= , CM000668.1:g.7565550G=	GRCh37
NC_000006.10:g.7510549G=	NCBI36
NG_008803.1:g.28681G= , LRG_423:g.28681G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.778-42G=	ENSP00000518230.1:n.778-42G=
ENST00000682228.1:n.60G=
ENST00000379802.8:c.778-42G= MANE Select	ENSP00000369129.3:n.778-42G=
ENST00000379802.7:c.778-42G=	ENSP00000369129.3:n.778-42G=
ENST00000418664.2:c.778-42G=	ENSP00000396591.2:n.778-42G=
ENST00000506617.1:n.296-42G=
NM_001008844.1:c.778-42G=	NP_001008844.1:n.778-42G=
NM_004415.2:c.778-42G= , LRG_423t1:c.778-42G=	NP_004406.2:n.778-42G=
XM_011514323.1:c.778-42G=	XP_011512625.1:n.778-42G=
NM_001008844.2:c.778-42G=	NP_001008844.1:n.778-42G=
NM_001319034.1:c.778-42G=	NP_001305963.1:n.778-42G=
NM_004415.3:c.778-42G=	NP_004406.2:n.778-42G=
NM_004415.4:c.778-42G= MANE Select	NP_004406.2:n.778-42G=
NM_001008844.3:c.778-42G=	NP_001008844.1:n.778-42G=
NM_001319034.2:c.778-42G=	NP_001305963.1:n.778-42G=