Canonical Allele Identifier: CA050646
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs752665939
gnomAD v2: 6-7585255-A-G
gnomAD v4: 6-7585022-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585022A>G , CM000668.2:g.7585022A>G GRCh38
NC_000006.11:g.7585255A>G , CM000668.1:g.7585255A>G GRCh37
NC_000006.10:g.7530254A>G NCBI36
NG_008803.1:g.48386A>G , LRG_423:g.48386A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6431A>G ENSP00000518230.1:p.His2144Arg
ENST00000379802.8:c.7760A>G MANE Select ENSP00000369129.3:p.His2587Arg
ENST00000379802.7:c.7760A>G ENSP00000369129.3:p.His2587Arg
ENST00000418664.2:c.5963A>G ENSP00000396591.2:p.His1988Arg
NM_001008844.1:c.5963A>G NP_001008844.1:p.His1988Arg
NM_004415.2:c.7760A>G , LRG_423t1:c.7760A>G NP_004406.2:p.His2587Arg
XM_011514323.1:c.6431A>G XP_011512625.1:p.His2144Arg
NM_001008844.2:c.5963A>G NP_001008844.1:p.His1988Arg
NM_001319034.1:c.6431A>G NP_001305963.1:p.His2144Arg
NM_004415.3:c.7760A>G NP_004406.2:p.His2587Arg
NM_004415.4:c.7760A>G MANE Select NP_004406.2:p.His2587Arg
NM_001008844.3:c.5963A>G NP_001008844.1:p.His1988Arg
NM_001319034.2:c.6431A>G NP_001305963.1:p.His2144Arg