Canonical Allele Identifier: CA004272
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44896
ClinVar RCV Id: RCV000038031
dbSNP Id: rs397516933
gnomAD v4: 6-7580019-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7580019C>T , CM000668.2:g.7580019C>T GRCh38
NC_000006.11:g.7580252C>T , CM000668.1:g.7580252C>T GRCh37
NC_000006.10:g.7525251C>T NCBI36
NG_008803.1:g.43383C>T , LRG_423:g.43383C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.3829C>T ENSP00000518230.1:p.Gln1277Ter
ENST00000379802.8:c.3829C>T MANE Select ENSP00000369129.3:p.Gln1277Ter
ENST00000379802.7:c.3829C>T ENSP00000369129.3:p.Gln1277Ter
ENST00000418664.2:c.3582+247C>T ENSP00000396591.2:n.3582+247C>T
NM_001008844.1:c.3582+247C>T NP_001008844.1:n.3582+247C>T
NM_004415.2:c.3829C>T , LRG_423t1:c.3829C>T NP_004406.2:p.Gln1277Ter
XM_011514323.1:c.3829C>T XP_011512625.1:p.Gln1277Ter
NM_001008844.2:c.3582+247C>T NP_001008844.1:n.3582+247C>T
NM_001319034.1:c.3829C>T NP_001305963.1:p.Gln1277Ter
NM_004415.3:c.3829C>T NP_004406.2:p.Gln1277Ter
NM_004415.4:c.3829C>T MANE Select NP_004406.2:p.Gln1277Ter
NM_001008844.3:c.3582+247C>T NP_001008844.1:n.3582+247C>T
NM_001319034.2:c.3829C>T NP_001305963.1:p.Gln1277Ter