Canonical Allele Identifier: CA1608608115

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583443C= , CM000668.2:g.7583443C=	GRCh38
NC_000006.11:g.7583676C= , CM000668.1:g.7583676C=	GRCh37
NC_000006.10:g.7528675C=	NCBI36
NG_008803.1:g.46807C= , LRG_423:g.46807C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4852C=	ENSP00000518230.1:p.Pro1618=
ENST00000379802.8:c.6181C= MANE Select	ENSP00000369129.3:p.Pro2061=
ENST00000379802.7:c.6181C=	ENSP00000369129.3:p.Pro2061=
ENST00000418664.2:c.4384C=	ENSP00000396591.2:p.Pro1462=
NM_001008844.1:c.4384C=	NP_001008844.1:p.Pro1462=
NM_004415.2:c.6181C= , LRG_423t1:c.6181C=	NP_004406.2:p.Pro2061=
XM_011514323.1:c.4852C=	XP_011512625.1:p.Pro1618=
NM_001008844.2:c.4384C=	NP_001008844.1:p.Pro1462=
NM_001319034.1:c.4852C=	NP_001305963.1:p.Pro1618=
NM_004415.3:c.6181C=	NP_004406.2:p.Pro2061=
NM_004415.4:c.6181C= MANE Select	NP_004406.2:p.Pro2061=
NM_001008844.3:c.4384C=	NP_001008844.1:p.Pro1462=
NM_001319034.2:c.4852C=	NP_001305963.1:p.Pro1618=