Canonical Allele Identifier: CA1608613473

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585162A= , CM000668.2:g.7585162A=	GRCh38
NC_000006.11:g.7585395A= , CM000668.1:g.7585395A=	GRCh37
NC_000006.10:g.7530394A=	NCBI36
NG_008803.1:g.48526A= , LRG_423:g.48526A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6571A=	ENSP00000518230.1:p.Thr2191=
ENST00000379802.8:c.7900A= MANE Select	ENSP00000369129.3:p.Thr2634=
ENST00000379802.7:c.7900A=	ENSP00000369129.3:p.Thr2634=
ENST00000418664.2:c.6103A=	ENSP00000396591.2:p.Thr2035=
NM_001008844.1:c.6103A=	NP_001008844.1:p.Thr2035=
NM_004415.2:c.7900A= , LRG_423t1:c.7900A=	NP_004406.2:p.Thr2634=
XM_011514323.1:c.6571A=	XP_011512625.1:p.Thr2191=
NM_001008844.2:c.6103A=	NP_001008844.1:p.Thr2035=
NM_001319034.1:c.6571A=	NP_001305963.1:p.Thr2191=
NM_004415.3:c.7900A=	NP_004406.2:p.Thr2634=
NM_004415.4:c.7900A= MANE Select	NP_004406.2:p.Thr2634=
NM_001008844.3:c.6103A=	NP_001008844.1:p.Thr2035=
NM_001319034.2:c.6571A=	NP_001305963.1:p.Thr2191=