Canonical Allele Identifier: CA1608606834

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7582979T= , CM000668.2:g.7582979T=	GRCh38
NC_000006.11:g.7583212T= , CM000668.1:g.7583212T=	GRCh37
NC_000006.10:g.7528211T=	NCBI36
NG_008803.1:g.46343T= , LRG_423:g.46343T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4388T=	ENSP00000518230.1:p.Ile1463=
ENST00000379802.8:c.5717T= MANE Select	ENSP00000369129.3:p.Ile1906=
ENST00000379802.7:c.5717T=	ENSP00000369129.3:p.Ile1906=
ENST00000418664.2:c.3920T=	ENSP00000396591.2:p.Ile1307=
NM_001008844.1:c.3920T=	NP_001008844.1:p.Ile1307=
NM_004415.2:c.5717T= , LRG_423t1:c.5717T=	NP_004406.2:p.Ile1906=
XM_011514323.1:c.4388T=	XP_011512625.1:p.Ile1463=
NM_001008844.2:c.3920T=	NP_001008844.1:p.Ile1307=
NM_001319034.1:c.4388T=	NP_001305963.1:p.Ile1463=
NM_004415.3:c.5717T=	NP_004406.2:p.Ile1906=
NM_004415.4:c.5717T= MANE Select	NP_004406.2:p.Ile1906=
NM_001008844.3:c.3920T=	NP_001008844.1:p.Ile1307=
NM_001319034.2:c.4388T=	NP_001305963.1:p.Ile1463=