Canonical Allele Identifier: CA1608607915
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583362G= , CM000668.2:g.7583362G= GRCh38
NC_000006.11:g.7583595G= , CM000668.1:g.7583595G= GRCh37
NC_000006.10:g.7528594G= NCBI36
NG_008803.1:g.46726G= , LRG_423:g.46726G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.4771G= ENSP00000518230.1:p.Ala1591=
ENST00000379802.8:c.6100G= MANE Select ENSP00000369129.3:p.Ala2034=
ENST00000379802.7:c.6100G= ENSP00000369129.3:p.Ala2034=
ENST00000418664.2:c.4303G= ENSP00000396591.2:p.Ala1435=
NM_001008844.1:c.4303G= NP_001008844.1:p.Ala1435=
NM_004415.2:c.6100G= , LRG_423t1:c.6100G= NP_004406.2:p.Ala2034=
XM_011514323.1:c.4771G= XP_011512625.1:p.Ala1591=
NM_001008844.2:c.4303G= NP_001008844.1:p.Ala1435=
NM_001319034.1:c.4771G= NP_001305963.1:p.Ala1591=
NM_004415.3:c.6100G= NP_004406.2:p.Ala2034=
NM_004415.4:c.6100G= MANE Select NP_004406.2:p.Ala2034=
NM_001008844.3:c.4303G= NP_001008844.1:p.Ala1435=
NM_001319034.2:c.4771G= NP_001305963.1:p.Ala1591=