Canonical Allele Identifier: CA2677223577
Gene: DSP HGNC NCBI

Linked Data

gnomAD v4: 6-7576853-TA-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7576856del , CM000668.2:g.7576856del GRCh38
NC_000006.11:g.7577089del , CM000668.1:g.7577089del GRCh37
NC_000006.10:g.7522088del NCBI36
NG_008803.1:g.40220del , LRG_423:g.40220del

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.2794-103del ENSP00000518230.1:n.2794-103del
ENST00000379802.8:c.2794-103del MANE Select ENSP00000369129.3:n.2794-103del
ENST00000379802.7:c.2794-103del ENSP00000369129.3:n.2794-103del
ENST00000418664.2:c.2794-103del ENSP00000396591.2:n.2794-103del
NM_001008844.1:c.2794-103del NP_001008844.1:n.2794-103del
NM_004415.2:c.2794-103del , LRG_423t1:c.2794-103del NP_004406.2:n.2794-103del
XM_011514323.1:c.2794-103del XP_011512625.1:n.2794-103del
NM_001008844.2:c.2794-103del NP_001008844.1:n.2794-103del
NM_001319034.1:c.2794-103del NP_001305963.1:n.2794-103del
NM_004415.3:c.2794-103del NP_004406.2:n.2794-103del
NM_004415.4:c.2794-103del MANE Select NP_004406.2:n.2794-103del
NM_001008844.3:c.2794-103del NP_001008844.1:n.2794-103del
NM_001319034.2:c.2794-103del NP_001305963.1:n.2794-103del