Canonical Allele Identifier: CA2677219490
Gene: DSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7565268_7565274del , CM000668.2:g.7565268_7565274del GRCh38
NC_000006.11:g.7565501_7565507del , CM000668.1:g.7565501_7565507del GRCh37
NC_000006.10:g.7510500_7510506del NCBI36
NG_008803.1:g.28632_28638del , LRG_423:g.28632_28638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.778-91_778-85del ENSP00000518230.1:n.778-91_778-85del
ENST00000682228.1:n.11_17del
ENST00000379802.8:c.778-91_778-85del MANE Select ENSP00000369129.3:n.778-91_778-85del
ENST00000379802.7:c.778-91_778-85del ENSP00000369129.3:n.778-91_778-85del
ENST00000418664.2:c.778-91_778-85del ENSP00000396591.2:n.778-91_778-85del
ENST00000506617.1:n.296-91_296-85del
NM_001008844.1:c.778-91_778-85del NP_001008844.1:n.778-91_778-85del
NM_004415.2:c.778-91_778-85del , LRG_423t1:c.778-91_778-85del NP_004406.2:n.778-91_778-85del
XM_011514323.1:c.778-91_778-85del XP_011512625.1:n.778-91_778-85del
NM_001008844.2:c.778-91_778-85del NP_001008844.1:n.778-91_778-85del
NM_001319034.1:c.778-91_778-85del NP_001305963.1:n.778-91_778-85del
NM_004415.3:c.778-91_778-85del NP_004406.2:n.778-91_778-85del
NM_004415.4:c.778-91_778-85del MANE Select NP_004406.2:n.778-91_778-85del
NM_001008844.3:c.778-91_778-85del NP_001008844.1:n.778-91_778-85del
NM_001319034.2:c.778-91_778-85del NP_001305963.1:n.778-91_778-85del