Canonical Allele Identifier: CA1608621235
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7567659_7567660delinsAT , CM000668.2:g.7567659_7567660delinsAT GRCh38
NC_000006.11:g.7567892_7567893delinsAT , CM000668.1:g.7567892_7567893delinsAT GRCh37
NC_000006.10:g.7512891_7512892delinsAT NCBI36
NG_008803.1:g.31023_31024delinsAT , LRG_423:g.31023_31024delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.1141-122_1141-121delinsAT ENSP00000518230.1:n.1141-122_1141-121delinsAT
ENST00000682228.1:n.674_675delinsAT
ENST00000379802.8:c.1141-122_1141-121delinsAT MANE Select ENSP00000369129.3:n.1141-122_1141-121delinsAT
ENST00000379802.7:c.1141-122_1141-121delinsAT ENSP00000369129.3:n.1141-122_1141-121delinsAT
ENST00000418664.2:c.1141-122_1141-121delinsAT ENSP00000396591.2:n.1141-122_1141-121delinsAT
NM_001008844.1:c.1141-122_1141-121delinsAT NP_001008844.1:n.1141-122_1141-121delinsAT
NM_004415.2:c.1141-122_1141-121delinsAT , LRG_423t1:c.1141-122_1141-121delinsAT NP_004406.2:n.1141-122_1141-121delinsAT
XM_011514323.1:c.1141-122_1141-121delinsAT XP_011512625.1:n.1141-122_1141-121delinsAT
NM_001008844.2:c.1141-122_1141-121delinsAT NP_001008844.1:n.1141-122_1141-121delinsAT
NM_001319034.1:c.1141-122_1141-121delinsAT NP_001305963.1:n.1141-122_1141-121delinsAT
NM_004415.3:c.1141-122_1141-121delinsAT NP_004406.2:n.1141-122_1141-121delinsAT
NM_004415.4:c.1141-122_1141-121delinsAT MANE Select NP_004406.2:n.1141-122_1141-121delinsAT
NM_001008844.3:c.1141-122_1141-121delinsAT NP_001008844.1:n.1141-122_1141-121delinsAT
NM_001319034.2:c.1141-122_1141-121delinsAT NP_001305963.1:n.1141-122_1141-121delinsAT