Canonical Allele Identifier: CA1608613607
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585193G= , CM000668.2:g.7585193G= GRCh38
NC_000006.11:g.7585426G= , CM000668.1:g.7585426G= GRCh37
NC_000006.10:g.7530425G= NCBI36
NG_008803.1:g.48557G= , LRG_423:g.48557G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6602G= ENSP00000518230.1:p.Ser2201=
ENST00000379802.8:c.7931G= MANE Select ENSP00000369129.3:p.Ser2644=
ENST00000379802.7:c.7931G= ENSP00000369129.3:p.Ser2644=
ENST00000418664.2:c.6134G= ENSP00000396591.2:p.Ser2045=
NM_001008844.1:c.6134G= NP_001008844.1:p.Ser2045=
NM_004415.2:c.7931G= , LRG_423t1:c.7931G= NP_004406.2:p.Ser2644=
XM_011514323.1:c.6602G= XP_011512625.1:p.Ser2201=
NM_001008844.2:c.6134G= NP_001008844.1:p.Ser2045=
NM_001319034.1:c.6602G= NP_001305963.1:p.Ser2201=
NM_004415.3:c.7931G= NP_004406.2:p.Ser2644=
NM_004415.4:c.7931G= MANE Select NP_004406.2:p.Ser2644=
NM_001008844.3:c.6134G= NP_001008844.1:p.Ser2045=
NM_001319034.2:c.6602G= NP_001305963.1:p.Ser2201=