Canonical Allele Identifier: CA1608614997

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585586C= , CM000668.2:g.7585586C=	GRCh38
NC_000006.11:g.7585819C= , CM000668.1:g.7585819C=	GRCh37
NC_000006.10:g.7530818C=	NCBI36
NG_008803.1:g.48950C= , LRG_423:g.48950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6995C=	ENSP00000518230.1:p.Thr2332=
ENST00000379802.8:c.8324C= MANE Select	ENSP00000369129.3:p.Thr2775=
ENST00000379802.7:c.8324C=	ENSP00000369129.3:p.Thr2775=
ENST00000418664.2:c.6527C=	ENSP00000396591.2:p.Thr2176=
NM_001008844.1:c.6527C=	NP_001008844.1:p.Thr2176=
NM_004415.2:c.8324C= , LRG_423t1:c.8324C=	NP_004406.2:p.Thr2775=
XM_011514323.1:c.6995C=	XP_011512625.1:p.Thr2332=
NM_001008844.2:c.6527C=	NP_001008844.1:p.Thr2176=
NM_001319034.1:c.6995C=	NP_001305963.1:p.Thr2332=
NM_004415.3:c.8324C=	NP_004406.2:p.Thr2775=
NM_004415.4:c.8324C= MANE Select	NP_004406.2:p.Thr2775=
NM_001008844.3:c.6527C=	NP_001008844.1:p.Thr2176=
NM_001319034.2:c.6995C=	NP_001305963.1:p.Thr2332=