Canonical Allele Identifier: CA1608607900
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583354T= , CM000668.2:g.7583354T= GRCh38
NC_000006.11:g.7583587T= , CM000668.1:g.7583587T= GRCh37
NC_000006.10:g.7528586T= NCBI36
NG_008803.1:g.46718T= , LRG_423:g.46718T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.4763T= ENSP00000518230.1:p.Leu1588=
ENST00000379802.8:c.6092T= MANE Select ENSP00000369129.3:p.Leu2031=
ENST00000379802.7:c.6092T= ENSP00000369129.3:p.Leu2031=
ENST00000418664.2:c.4295T= ENSP00000396591.2:p.Leu1432=
NM_001008844.1:c.4295T= NP_001008844.1:p.Leu1432=
NM_004415.2:c.6092T= , LRG_423t1:c.6092T= NP_004406.2:p.Leu2031=
XM_011514323.1:c.4763T= XP_011512625.1:p.Leu1588=
NM_001008844.2:c.4295T= NP_001008844.1:p.Leu1432=
NM_001319034.1:c.4763T= NP_001305963.1:p.Leu1588=
NM_004415.3:c.6092T= NP_004406.2:p.Leu2031=
NM_004415.4:c.6092T= MANE Select NP_004406.2:p.Leu2031=
NM_001008844.3:c.4295T= NP_001008844.1:p.Leu1432=
NM_001319034.2:c.4763T= NP_001305963.1:p.Leu1588=