Canonical Allele Identifier: CA053451
Community Standard Title: NM_004415.4(DSP):c.998G>A (p.Ser333Asn)
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7566435G>A , CM000668.2:g.7566435G>A GRCh38
NC_000006.11:g.7566668G>A , CM000668.1:g.7566668G>A GRCh37
NC_000006.10:g.7511667G>A NCBI36
NG_008803.1:g.29799G>A , LRG_423:g.29799G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004415.4:c.998G>A MANE Select NP_004406.2:p.Ser333Asn
ENST00000379802.8:c.998G>A MANE Select ENSP00000369129.3:p.Ser333Asn
NM_001008844.1:c.998G>A NP_001008844.1:p.Ser333Asn
NM_001008844.2:c.998G>A NP_001008844.1:p.Ser333Asn
NM_001008844.3:c.998G>A NP_001008844.1:p.Ser333Asn
NM_001319034.1:c.998G>A NP_001305963.1:p.Ser333Asn
NM_001319034.2:c.998G>A NP_001305963.1:p.Ser333Asn
NM_004415.2:c.998G>A , LRG_423t1:c.998G>A NP_004406.2:p.Ser333Asn
NM_004415.3:c.998G>A NP_004406.2:p.Ser333Asn
ENST00000379802.7:c.998G>A ENSP00000369129.3:p.Ser333Asn
ENST00000418664.2:c.998G>A ENSP00000396591.2:p.Ser333Asn
ENST00000682228.1:n.322G>A
ENST00000710359.1:c.998G>A ENSP00000518230.1:p.Ser333Asn
XM_011514323.1:c.998G>A XP_011512625.1:p.Ser333Asn