Canonical Allele Identifier: CA046745
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs760673242
gnomAD v2: 6-7583557-C-A
gnomAD v4: 6-7583324-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583324C>A , CM000668.2:g.7583324C>A GRCh38
NC_000006.11:g.7583557C>A , CM000668.1:g.7583557C>A GRCh37
NC_000006.10:g.7528556C>A NCBI36
NG_008803.1:g.46688C>A , LRG_423:g.46688C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4733C>A ENSP00000518230.1:p.Ala1578Glu
ENST00000379802.8:c.6062C>A MANE Select ENSP00000369129.3:p.Ala2021Glu
ENST00000379802.7:c.6062C>A ENSP00000369129.3:p.Ala2021Glu
ENST00000418664.2:c.4265C>A ENSP00000396591.2:p.Ala1422Glu
NM_001008844.1:c.4265C>A NP_001008844.1:p.Ala1422Glu
NM_004415.2:c.6062C>A , LRG_423t1:c.6062C>A NP_004406.2:p.Ala2021Glu
XM_011514323.1:c.4733C>A XP_011512625.1:p.Ala1578Glu
NM_001008844.2:c.4265C>A NP_001008844.1:p.Ala1422Glu
NM_001319034.1:c.4733C>A NP_001305963.1:p.Ala1578Glu
NM_004415.3:c.6062C>A NP_004406.2:p.Ala2021Glu
NM_004415.4:c.6062C>A MANE Select NP_004406.2:p.Ala2021Glu
NM_001008844.3:c.4265C>A NP_001008844.1:p.Ala1422Glu
NM_001319034.2:c.4733C>A NP_001305963.1:p.Ala1578Glu