Canonical Allele Identifier: CA1608608283

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583491C= , CM000668.2:g.7583491C=	GRCh38
NC_000006.11:g.7583724C= , CM000668.1:g.7583724C=	GRCh37
NC_000006.10:g.7528723C=	NCBI36
NG_008803.1:g.46855C= , LRG_423:g.46855C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.4900C=	ENSP00000518230.1:p.Leu1634=
ENST00000379802.8:c.6229C= MANE Select	ENSP00000369129.3:p.Leu2077=
ENST00000379802.7:c.6229C=	ENSP00000369129.3:p.Leu2077=
ENST00000418664.2:c.4432C=	ENSP00000396591.2:p.Leu1478=
NM_001008844.1:c.4432C=	NP_001008844.1:p.Leu1478=
NM_004415.2:c.6229C= , LRG_423t1:c.6229C=	NP_004406.2:p.Leu2077=
XM_011514323.1:c.4900C=	XP_011512625.1:p.Leu1634=
NM_001008844.2:c.4432C=	NP_001008844.1:p.Leu1478=
NM_001319034.1:c.4900C=	NP_001305963.1:p.Leu1634=
NM_004415.3:c.6229C=	NP_004406.2:p.Leu2077=
NM_004415.4:c.6229C= MANE Select	NP_004406.2:p.Leu2077=
NM_001008844.3:c.4432C=	NP_001008844.1:p.Leu1478=
NM_001319034.2:c.4900C=	NP_001305963.1:p.Leu1634=