Canonical Allele Identifier: CA052478
Community Standard Title: NM_004415.4(DSP):c.8482G>A (p.Gly2828Ser)
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585744G>A , CM000668.2:g.7585744G>A GRCh38
NC_000006.11:g.7585977G>A , CM000668.1:g.7585977G>A GRCh37
NC_000006.10:g.7530976G>A NCBI36
NG_008803.1:g.49108G>A , LRG_423:g.49108G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004415.4:c.8482G>A MANE Select NP_004406.2:p.Gly2828Ser
ENST00000379802.8:c.8482G>A MANE Select ENSP00000369129.3:p.Gly2828Ser
NM_001008844.1:c.6685G>A NP_001008844.1:p.Gly2229Ser
NM_001008844.2:c.6685G>A NP_001008844.1:p.Gly2229Ser
NM_001008844.3:c.6685G>A NP_001008844.1:p.Gly2229Ser
NM_001319034.1:c.7153G>A NP_001305963.1:p.Gly2385Ser
NM_001319034.2:c.7153G>A NP_001305963.1:p.Gly2385Ser
NM_004415.2:c.8482G>A , LRG_423t1:c.8482G>A NP_004406.2:p.Gly2828Ser
NM_004415.3:c.8482G>A NP_004406.2:p.Gly2828Ser
ENST00000379802.7:c.8482G>A ENSP00000369129.3:p.Gly2828Ser
ENST00000418664.2:c.6685G>A ENSP00000396591.2:p.Gly2229Ser
ENST00000710359.1:c.7153G>A ENSP00000518230.1:p.Gly2385Ser
XM_011514323.1:c.7153G>A XP_011512625.1:p.Gly2385Ser