Canonical Allele Identifier: CA1608613100

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585046C= , CM000668.2:g.7585046C=	GRCh38
NC_000006.11:g.7585279C= , CM000668.1:g.7585279C=	GRCh37
NC_000006.10:g.7530278C=	NCBI36
NG_008803.1:g.48410C= , LRG_423:g.48410C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6455C=	ENSP00000518230.1:p.Thr2152=
ENST00000379802.8:c.7784C= MANE Select	ENSP00000369129.3:p.Thr2595=
ENST00000379802.7:c.7784C=	ENSP00000369129.3:p.Thr2595=
ENST00000418664.2:c.5987C=	ENSP00000396591.2:p.Thr1996=
NM_001008844.1:c.5987C=	NP_001008844.1:p.Thr1996=
NM_004415.2:c.7784C= , LRG_423t1:c.7784C=	NP_004406.2:p.Thr2595=
XM_011514323.1:c.6455C=	XP_011512625.1:p.Thr2152=
NM_001008844.2:c.5987C=	NP_001008844.1:p.Thr1996=
NM_001319034.1:c.6455C=	NP_001305963.1:p.Thr2152=
NM_004415.3:c.7784C=	NP_004406.2:p.Thr2595=
NM_004415.4:c.7784C= MANE Select	NP_004406.2:p.Thr2595=
NM_001008844.3:c.5987C=	NP_001008844.1:p.Thr1996=
NM_001319034.2:c.6455C=	NP_001305963.1:p.Thr2152=