Canonical Allele Identifier: CA1608623761
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7568883_7568888delinsTAAAAG , CM000668.2:g.7568883_7568888delinsTAAAAG GRCh38
NC_000006.11:g.7569116_7569121delinsTAAAAG , CM000668.1:g.7569116_7569121delinsTAAAAG GRCh37
NC_000006.10:g.7514115_7514120delinsTAAAAG NCBI36
NG_008803.1:g.32247_32252delinsTAAAAG , LRG_423:g.32247_32252delinsTAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.1419+294_1420-298delinsTAAAAG ENSP00000518230.1:n.1419+294_1420-298delinsTAAAAG
ENST00000379802.8:c.1419+294_1420-298delinsTAAAAG MANE Select ENSP00000369129.3:n.1419+294_1420-298delinsTAAAAG
ENST00000379802.7:c.1419+294_1420-298delinsTAAAAG ENSP00000369129.3:n.1419+294_1420-298delinsTAAAAG
ENST00000418664.2:c.1419+294_1420-298delinsTAAAAG ENSP00000396591.2:n.1419+294_1420-298delinsTAAAAG
NM_001008844.1:c.1419+294_1420-298delinsTAAAAG NP_001008844.1:n.1419+294_1420-298delinsTAAAAG
NM_004415.2:c.1419+294_1420-298delinsTAAAAG , LRG_423t1:c.1419+294_1420-298delinsTAAAAG NP_004406.2:n.1419+294_1420-298delinsTAAAAG
XM_011514323.1:c.1419+294_1420-298delinsTAAAAG XP_011512625.1:n.1419+294_1420-298delinsTAAAAG
NM_001008844.2:c.1419+294_1420-298delinsTAAAAG NP_001008844.1:n.1419+294_1420-298delinsTAAAAG
NM_001319034.1:c.1419+294_1420-298delinsTAAAAG NP_001305963.1:n.1419+294_1420-298delinsTAAAAG
NM_004415.3:c.1419+294_1420-298delinsTAAAAG NP_004406.2:n.1419+294_1420-298delinsTAAAAG
NM_004415.4:c.1419+294_1420-298delinsTAAAAG MANE Select NP_004406.2:n.1419+294_1420-298delinsTAAAAG
NM_001008844.3:c.1419+294_1420-298delinsTAAAAG NP_001008844.1:n.1419+294_1420-298delinsTAAAAG
NM_001319034.2:c.1419+294_1420-298delinsTAAAAG NP_001305963.1:n.1419+294_1420-298delinsTAAAAG