Canonical Allele Identifier: CA1608611344
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7584511G= , CM000668.2:g.7584511G= GRCh38
NC_000006.11:g.7584744G= , CM000668.1:g.7584744G= GRCh37
NC_000006.10:g.7529743G= NCBI36
NG_008803.1:g.47875G= , LRG_423:g.47875G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.5920G= ENSP00000518230.1:p.Asp1974=
ENST00000379802.8:c.7249G= MANE Select ENSP00000369129.3:p.Asp2417=
ENST00000379802.7:c.7249G= ENSP00000369129.3:p.Asp2417=
ENST00000418664.2:c.5452G= ENSP00000396591.2:p.Asp1818=
NM_001008844.1:c.5452G= NP_001008844.1:p.Asp1818=
NM_004415.2:c.7249G= , LRG_423t1:c.7249G= NP_004406.2:p.Asp2417=
XM_011514323.1:c.5920G= XP_011512625.1:p.Asp1974=
NM_001008844.2:c.5452G= NP_001008844.1:p.Asp1818=
NM_001319034.1:c.5920G= NP_001305963.1:p.Asp1974=
NM_004415.3:c.7249G= NP_004406.2:p.Asp2417=
NM_004415.4:c.7249G= MANE Select NP_004406.2:p.Asp2417=
NM_001008844.3:c.5452G= NP_001008844.1:p.Asp1818=
NM_001319034.2:c.5920G= NP_001305963.1:p.Asp1974=